CPT 81405 Fee Schedule
Last Verified: August 2026
Healthcare providers use this code to document and receive reimbursement for visits that address moderate-level medical decision-making, often including multiple diagnoses or prescription management.
Mopath Procedure Level 6, Molecular Pathology Procedure Level 6 (Eg Analysis Of 6-10 Exons By Dna Sequence Analysis Mutation Scanning Or Duplication Deletion Variants Of 11-25 Exons Regionally Targeted Cytogenomic Array Analysis) Abcd1 (Atp-Binding Cassette Sub-Family D [Ald] Member 1) (Eg Adrenoleukodystrophy) Full Gene Sequence Acads (Acyl-Coa Dehydrogenase C-2 To C-3 Short Chain) (Eg Short Chain Acyl-Coa Dehydrogenase Deficiency) Full Gene Sequence Acta2 (Actin Alpha 2 Smooth Muscle Aorta) (Eg Thoracic Aortic Aneurysms And Aortic Dissections) Full Gene Sequence Actc1 (Actin Alpha Cardiac Muscle 1) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Ankrd1 (Ankyrin Repeat Domain 1) (Eg Dilated Cardiomyopathy) Full Gene Sequence Aptx (Aprataxin) (Eg Ataxia With Oculomotor Apraxia 1) Full Gene Sequence Arsa (Arylsulfatase A) (Eg Arylsulfatase A Deficiency) Full Gene Sequence Bckdha (Branched Chain Keto Acid Dehydrogenase E1 Alpha Polypeptide) (Eg Maple Syrup Urine Disease Type 1a) Full Gene Sequence Bcs1l (Bcs1-Like [S. Cerevisiae]) (Eg Leigh Syndrome Mitochondrial Complex Iii Deficiency Gracile Syndrome) Full Gene Sequence Bmpr2 (Bone Morphogenetic Protein Receptor Type Ii [Serine Threonine Kinase]) (Eg Heritable Pulmonary Arterial Hypertension) Duplication Deletion Analysis Casq2 (Calsequestrin 2 [Cardiac Muscle]) (Eg Catecholaminergic Polymorphic Ventricular Tachycardia) Full Gene Sequence Casr (Calcium-Sensing Receptor) (Eg Hypocalcemia) Full Gene Sequence Cdkl5 (Cyclin-Dependent Kinase-Like 5) (Eg Early Infantile Epileptic Encephalopathy) Duplication Deletion Analysis Chrna4 (Cholinergic Receptor Nicotinic Alpha 4) (Eg Nocturnal Frontal Lobe Epilepsy) Full Gene Sequence Chrnb2 (Cholinergic Receptor Nicotinic Beta 2 [Neuronal]) (Eg Nocturnal Frontal Lobe Epilepsy) Full Gene Sequence Cox10 (Cox10 Homolog Cytochrome C Oxidase Assembly Protein) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Cox15 (Cox15 Homolog Cytochrome C Oxidase Assembly Protein) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Cpox (Coproporphyrinogen Oxidase) (Eg Hereditary Coproporphyria) Full Gene Sequence Ctrc (Chymotrypsin C) (Eg Hereditary Pancreatitis) Full Gene Sequence Cyp11b1 (Cytochrome P450 Family 11 Subfamily B Polypeptide 1) (Eg Congenital Adrenal Hyperplasia) Full Gene Sequence Cyp17a1 (Cytochrome P450 Family 17 Subfamily A Polypeptide 1) (Eg Congenital Adrenal Hyperplasia) Full Gene Sequence Cyp21a2 (Cytochrome P450 Family 21 Subfamily A Polypeptide2) (Eg Steroid 21-Hydroxylase Isoform Congenital Adrenal Hyperplasia) Full Gene Sequence Cytogenomic Constitutional Targeted Microarray Analysis Of Chromosome 22q13 By Interrogation Of Genomic Regions For Copy Number And Single Nucleotide Polymorphism (Snp) Variants For Chromosomal Abnormalities (When Performing Cytogenomic [Genome-Wide] Analysis For Constitutional Chromosomal Abnormalities See 81228 81229 81349) (Do Not Report Analyte-Specific Molecular Pathology Procedures Separately When The Specific Analytes Are Included As Part Of The Microarray Analysis Of Chromosome 22q13) (Do Not Report 88271 When Performing Cytogenomic Microarray Analysis) Dbt (Dihydrolipoamide Branched Chain Transacylase E2) (Eg Maple Syrup Urine Disease Type 2) Duplication Deletion Analysis Dcx (Doublecortin) (Eg X-Linked Lissencephaly) Full Gene Sequence Des (Desmin) (Eg Myofibrillar Myopathy) Full Gene Sequence Dfnb59 (Deafness Autosomal Recessive 59) (Eg Autosomal Recessive Nonsyndromic Hearing Impairment) Full Gene Sequence Dguok (Deoxyguanosine Kinase) (Eg Hepatocerebral Mitochondrial Dna Depletion Syndrome) Full Gene Sequence Dhcr7 (7-Dehydrocholesterol Reductase) (Eg Smith-Lemli-Opitz Syndrome) Full Gene Sequence Eif2b2 (Eukaryotic Translation Initiation Factor 2b Subunit 2 Beta 39kda) (Eg Leukoencephalopathy With Vanishing White Matter) Full Gene Sequence Emd (Emerin) (Eg Emery-Dreifuss Muscular Dystrophy) Full Gene Sequence Eng (Endoglin) (Eg Hereditary Hemorrhagic Telangiectasia Type 1) Duplication Deletion Analysis Eya1 (Eyes Absent Homolog 1 [Drosophila]) (Eg Branchio-Oto-Renal [Bor] Spectrum Disorders) Duplication Deletion Analysis Fgfr1 (Fibroblast Growth Factor Receptor 1) (Eg Kallmann Syndrome 2) Full Gene Sequence Fh (Fumarate Hydratase) (Eg Fumarate Hydratase Deficiency Hereditary Leiomyomatosis With Renal Cell Cancer) Full Gene Sequence Fktn (Fukutin) (Eg Limb-Girdle Muscular Dystrophy [Lgmd] Type 2m Or 2l) Full Gene Sequence Ftsj1 (Ftsj Rna 2-O-Methyltransferase 1) (Eg X-Linked Intellectual Disability 9) Duplication Deletion Analysis Gabrg2 (Gamma-Aminobutyric Acid [Gaba] A Receptor Gamma 2) (Eg Generalized Epilepsy With Febrile Seizures) Full Gene Sequence Gch1 (Gtp Cyclohydrolase 1) (Eg Autosomal Dominant Dopa-Responsive Dystonia) Full Gene Sequence Gdap1 (Ganglioside-Induced Differentiation-Associated Protein 1) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Gfap (Glial Fibrillary Acidic Protein) (Eg Alexander Disease) Full Gene Sequence Ghr (Growth Hormone Receptor) (Eg Laron Syndrome) Full Gene Sequence Ghrhr (Growth Hormone Releasing Hormone Receptor) (Eg Growth Hormone Deficiency) Full Gene Sequence Gla (Galactosidase Alpha) (Eg Fabry Disease) Full Gene Sequence Hnf1a (Hnf1 Homeobox A) (Eg Maturity-Onset Diabetes Of The Young [Mody]) Full Gene Sequence Hnf1b (Hnf1 Homeobox B) (Eg Maturity-Onset Diabetes Of The Young [Mody]) Full Gene Sequence Htra1 (Htra Serine Peptidase 1) (Eg Macular Degeneration) Full Gene Sequence Ids (Iduronate 2-Sulfatase) (Eg Mucopolysacchridosis Type Ii) Full Gene Sequence Il2rg (Interleukin 2 Receptor Gamma) (Eg X-Linked Severe Combined Immunodeficiency) Full Gene Sequence Ispd (Isoprenoid Synthase Domain Containing) (Eg Muscle-Eye-Brain Disease Walker-Warburg Syndrome) Full Gene Sequence Kras (Kirsten Rat Sarcoma Viral Oncogene Homolog) (Eg Noonan Syndrome) Full Gene Sequence Lamp2 (Lysosomal-Associated Membrane Protein 2) (Eg Danon Disease) Full Gene Sequence Ldlr (Low Density Lipoprotein Receptor) (Eg Familial Hypercholesterolemia) Duplication Deletion Analysis Men1 (Multiple Endocrine Neoplasia I) (Eg Multiple Endocrine Neoplasia Type 1 Wermer Syndrome) Full Gene Sequence Mmaa (Methylmalonic Aciduria [Cobalamine Deficiency] Type A) (Eg Mmaa-Related Methylmalonic Acidemia) Full Gene Sequence Mmab (Methylmalonic Aciduria [Cobalamine Deficiency] Type B) (Eg Mmaa-Related Methylmalonic Acidemia) Full Gene Sequence Mpi (Mannose Phosphate Isomerase) (Eg Congenital Disorder Of Glycosylation 1b) Full Gene Sequence Mpv17 (Mpv17 Mitochondrial Inner Membrane Protein) (Eg Mitochondrial Dna Depletion Syndrome) Full Gene Sequence Mpz (Myelin Protein Zero) (Eg Charcot-Marie-Tooth) Full Gene Sequence Mtm1 (Myotubularin 1) (Eg X-Linked Centronuclear Myopathy) Duplication Deletion Analysis Myl2 (Myosin Light Chain 2 Regulatory Cardiac Slow) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Myl3 (Myosin Light Chain 3 Alkali Ventricular Skeletal Slow) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Myot (Myotilin) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Ndufs7 (Nadh Dehydrogenase [Ubiquinone] Fe-S Protein 7 20kda [Nadh-Coenzyme Q Reductase]) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Ndufs8 (Nadh Dehydrogenase [Ubiquinone] Fe-S Protein 8 23kda [Nadh-Coenzyme Q Reductase]) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Ndufv1 (Nadh Dehydrogenase [Ubiquinone] Flavoprotein 1 51kda) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Nefl (Neurofilament Light Polypeptide) (Eg Charcot-Marie-Tooth) Full Gene Sequence Nf2 (Neurofibromin 2 [Merlin]) (Eg Neurofibromatosis Type 2) Duplication Deletion Analysis Nlgn3 (Neuroligin 3) (Eg Autism Spectrum Disorders) Full Gene Sequence Nlgn4x (Neuroligin 4 X-Linked) (Eg Autism Spectrum Disorders) Full Gene Sequence Nphp1 (Nephronophthisis 1 [Juvenile]) (Eg Joubert Syndrome) Deletion Analysis And Duplication Analysis If Performed Nphs2 (Nephrosis 2 Idiopathic Steroid-Resistant [Podocin]) (Eg Steroid-Resistant Nephrotic Syndrome) Full Gene Sequence Nsd1 (Nuclear Receptor Binding Set Domain Protein 1) (Eg Sotos Syndrome) Duplication Deletion Analysis Otc (Ornithine Carbamoyltransferase) (Eg Ornithine Transcarbamylase Deficiency) Full Gene Sequence Pafah1b1 (Platelet-Activating Factor Acetylhydrolase 1b Regulatory Subunit 1 [45kda]) (Eg Lissencephaly Miller-Dieker Syndrome) Duplication Deletion Analysis Park2 (Parkinson Protein 2 E3 Ubiquitin Protein Ligase [Parkin]) (Eg Parkinson Disease) Duplication Deletion Analysis Pcca (Propionyl Coa Carboxylase Alpha Polypeptide) (Eg Propionic Acidemia Type 1) Duplication Deletion Analysis Pcdh19 (Protocadherin 19) (Eg Epileptic Encephalopathy) Full Gene Sequence Pdha1 (Pyruvate Dehydrogenase [Lipoamide] Alpha 1) (Eg Lactic Acidosis) Duplication Deletion Analysis Pdhb (Pyruvate Dehydrogenase [Lipoamide] Beta) (Eg Lactic Acidosis) Full Gene Sequence Pink1 (Pten Induced Putative Kinase 1) (Eg Parkinson Disease) Full Gene Sequence Pklr (Pyruvate Kinase Liver And Rbc) (Eg Pyruvate Kinase Deficiency) Full Gene Sequence Plp1 (Proteolipid Protein 1) (Eg Pelizaeus-Merzbacher Disease Spastic Paraplegia) Full Gene Sequence Pou1f1 (Pou Class 1 Homeobox 1) (Eg Combined Pituitary Hormone Deficiency) Full Gene Sequence Prx (Periaxin) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Pqbp1 (Polyglutamine Binding Protein 1) (Eg Renpenning Syndrome) Full Gene Sequence Psen1 (Presenilin 1) (Eg Alzheimer Disease) Full Gene Sequence Rab7a (Rab7a Member Ras Oncogene Family) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Rai1 (Retinoic Acid Induced 1) (Eg Smith-Magenis Syndrome) Full Gene Sequence Reep1 (Receptor Accessory Protein 1) (Eg Spastic Paraplegia) Full Gene Sequence Ret (Ret Proto-Oncogene) (Eg Multiple Endocrine Neoplasia Type 2a And Familial Medullary Thyroid Carcinoma) Targeted Sequence Analysis (Eg Exons 10 11 13-16) Rps19 (Ribosomal Protein S19) (Eg Diamond-Blackfan Anemia) Full Gene Sequence Rrm2b (Ribonucleotide Reductase M2 B [Tp53 Inducible]) (Eg Mitochondrial Dna Depletion) Full Gene Sequence Sco1 (Sco Cytochrome Oxidase Deficient Homolog 1) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Sdhb (Succinate Dehydrogenase Complex Subunit B Iron Sulfur) (Eg Hereditary Paraganglioma) Full Gene Sequence Sdhc (Succinate Dehydrogenase Complex Subunit C Integral Membrane Protein 15kda) (Eg Hereditary Paraganglioma-Pheochromocytoma Syndrome) Full Gene Sequence Sgca (Sarcoglycan Alpha [50kda Dystrophin-Associated Glycoprotein]) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Sgcb (Sarcoglycan Beta [43kda Dystrophin-Associated Glycoprotein]) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Sgcd (Sarcoglycan Delta [35kda Dystrophin-Associated Glycoprotein]) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Sgce (Sarcoglycan Epsilon) (Eg Myoclonic Dystonia) Duplication Deletion Analysis Sgcg (Sarcoglycan Gamma [35kda Dystrophin-Associated Glycoprotein]) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Shoc2 (Soc-2 Suppressor Of Clear Homolog) (Eg Noonan-Like Syndrome With Loose Anagen Hair) Full Gene Sequence Shox (Short Stature Homeobox) (Eg Langer Mesomelic Dysplasia) Full Gene Sequence Sil1 (Sil1 Homolog Endoplasmic Reticulum Chaperone [S. Cerevisiae]) (Eg Ataxia) Full Gene Sequence Slc2a1 (Solute Carrier Family 2 [Facilitated Glucose Transporter] Member 1) (Eg Glucose Transporter Type 1 [Glut 1] Deficiency Syndrome) Full Gene Sequence Slc16a2 (Solute Carrier Family 16 Member 2 [Thyroid Hormone Transporter]) (Eg Specific Thyroid Hormone Cell Transporter Deficiency Allan-Herndon-Dudley Syndrome) Full Gene Sequence Slc22a5 (Solute Carrier Family 22 [Organic Cation Carnitine Transporter] Member 5) (Eg Systemic Primary Carnitine Deficiency) Full Gene Sequence Slc25a20 (Solute Carrier Family 25 [Carnitine Acylcarnitine Translocase] Member 20) (Eg Carnitine-Acylcarnitine Translocase Deficiency) Full Gene Sequence Smad4 (Smad Family Member 4) (Eg Hemorrhagic Telangiectasia Syndrome Juvenile Polyposis) Duplication Deletion Analysis Spast (Spastin) (Eg Spastic Paraplegia) Duplication Deletion Analysis Spg7 (Spastic Paraplegia 7 [Pure And Complicated Autosomal Recessive]) (Eg Spastic Paraplegia) Duplication Deletion Analysis Spred1 (Sprouty-Related Evh1 Domain Containing 1) (Eg Legius Syndrome) Full Gene Sequence Stat3 (Signal Transducer And Activator Of Transcription 3 [Acute-Phase Response Factor]) (Eg Autosomal Dominant Hyper-Ige Syndrome) Targeted Sequence Analysis (Eg Exons 12 13 14 16 17 20 21) Stk11 (Serine Threonine Kinase 11) (Eg Peutz-Jeghers Syndrome) Full Gene Sequence Surf1 (Surfeit 1) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Tardbp (Tar Dna Binding Protein) (Eg Amyotrophic Lateral Sclerosis) Full Gene Sequence Tbx5 (T-Box 5) (Eg Holt-Oram Syndrome) Full Gene Sequence Tcf4 (Transcription Factor 4) (Eg Pitt-Hopkins Syndrome) Duplication Deletion Analysis Tgfbr1 (Transforming Growth Factor Beta Receptor 1) (Eg Marfan Syndrome) Full Gene Sequence Tgfbr2 (Transforming Growth Factor Beta Receptor 2) (Eg Marfan Syndrome) Full Gene Sequence Thrb (Thyroid Hormone Receptor Beta) (Eg Thyroid Hormone Resistance Thyroid Hormone Beta Receptor Deficiency) Full Gene Sequence Or Targeted Sequence Analysis Of >5 Exons Tk2 (Thymidine Kinase 2 Mitochondrial) (Eg Mitochondrial Dna Depletion Syndrome) Full Gene Sequence Tnnc1 (Troponin C Type 1 [Slow]) (Eg Hypertrophic Cardiomyopathy Or Dilated Cardiomyopathy) Full Gene Sequence Tnni3 (Troponin I Type 3 [Cardiac]) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Tpm1 (Tropomyosin 1 [Alpha]) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Tsc1 (Tuberous Sclerosis 1) (Eg Tuberous Sclerosis) Duplication Deletion Analysis Tymp (Thymidine Phosphorylase) (Eg Mitochondrial Dna Depletion Syndrome) Full Gene Sequence Vwf (Von Willebrand Factor) (Eg Von Willebrand Disease Type 2n) Targeted Sequence Analysis (Eg Exons 18-20 23-25) Wt1 (Wilms Tumor 1) (Eg Denys-Drash Syndrome Familial Wilms Tumor) Full Gene Sequence Zeb2 (Zinc Finger E-Box Binding Homeobox 2) (Eg Mowat-Wilson Syndrome) Full Gene Sequence
| Key Fact | Detail |
|---|---|
| Service Type | Pathology and Laboratory Procedures Molecular Pathology Procedures |
| Common Place of Service | 81 - Independent Laboratory 11 - Office |
| Common Modifiers | None 59 - Distinct Procedural Service XU - Unusual Non-Overlapping Service |
| Complexity Level | Moderate |
| Medicare Fee Schedule | View Medicare rates for 81405 |
National average reimbursement for CPT 81405 by major payers:
$278.82
$184.59
$274.94
$453.03
Preview provider-level rates for...
For billing codeCPT 81405
| Payer | Code | Rate | NPI | Tax ID | State | Specialty |
|---|---|---|---|---|---|---|
United | 81405 | $1653.68 | 1730616541 - BARRY TONG | 943281660 | CA | Genetic Counselor (M.S.) (170300000X) |
United | 81405 | $461.07 | 1164541181 - MATTHEW DEARDORFF | 953777340 - CHILDRENS HOSPITAL LOS ANGELES MEDICAL GROUP INC | CA | Clinical Genetics (M.D.) Physician (207SG0201X) |
United | 81405 | $488.67 | 1073054722 - HELIO COSTA | 770465765 | CA | Clinical Molecular Genetics Physician (207SG0203X) |
United | 81405 | $1050.98 | 1598141475 - MIGUEL DEL CAMPO CASANELLES | 330541971 | CA | Clinical Genetics (M.D.) Physician (207SG0201X) |
United | 81405 | $126.56 | 1508199621 - SERGE LARTCHENKO M.D., PLLC | 270839735 - (TX) SERGE LARTCHENKO MD PLLC | TX | General Acute Care Hospital (282N00000X) |
United | 81405 | $376.69 | 1649832353 - JOYCE SO | 943281666 | CA | Clinical Genetics (M.D.) Physician (207SG0201X) |
United | 81405 | $271.22 | 1740910330 - BRENDEN PHUNG | 621647259 - TENNESSEE ONCOLOGY PLLC | CA | Genetic Counselor (M.S.) (170300000X) |
United | 81405 | $126.56 | 1497821763 - VALERIE WATIKER | 880176637 - (NV) WM N EVANS M D LTD DBA CHILDRENS HEART CENTER | CA | Clinical Genetics (M.D.) Physician (207SG0201X) |
United | 81405 | $316.42 | 1972034841 - DAVID BLAIR | 943281666 | CA | Clinical Genetics (M.D.) Physician (207SG0201X) |
United | 81405 | $1488.31 | 1700425196 - LAURA CARDOSO | 943281662 | CA | Genetic Counselor (M.S.) (170300000X) |
United | 81405 | $301.35 | 1922058569 - SAN ANTONIO VAMC | 742112082 | TX | General Acute Care Hospital (282N00000X) |
United | 81405 | $126.56 | 1740453000 - GRAHAM REGIONAL MEDICAL CENTER, GRAHAM GENERAL HSOPITAL PHYSICIANS | 463113489 | TX | General Acute Care Hospital (282N00000X) |
United | 81405 | $461.07 | 1255916896 - BRIDGET FERNANDEZ | 820677283 - (CA) CHILDRENS HOSPITAL LOS ANGELES MEDICAL GROUP INC | CA | Clinical Genetics (M.D.) Physician (207SG0201X) |
United | 81405 | $376.69 | 1598113904 - ALICIA ORTA | 943281657 | CA | Genetic Counselor (M.S.) (170300000X) |
United | 81405 | $1488.31 | 1831403211 - HIND AL SAIF | 943281657 | CA | Clinical Genetics (M.D.) Physician (207SG0201X) |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
United | 99202 | $100.00 | 1234567890 | 1234567890 | CA | Cardiologist |
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CPT 81405 vs. Other Molecular Pathology Procedures Codes
The CPT 81405 code is part of the Pathology and Laboratory Procedures services used for Molecular Pathology Procedures. It represents a moderate-complexity encounter and is one of several codes that vary based on time spent, level of medical decision-making, and documentation requirements.
The CPT 81405 code involves more provider time and moderate medical decision-making, unlike lower-level codes that require less time and simpler assessments. It typically includes multiple diagnoses, medication management, or test interpretation, leading to higher reimbursement and more detailed documentation requirements.
| Code | Complexity | Description |
|---|---|---|
| 81404-CPT | Moderate | Mopath Procedure Level 5, Molecular Pathology Procedure Level 5 (Eg Analysis Of 2-5 Exons By Dna Sequence Analysis Mutation Scanning Or Duplication Deletion Variants Of 6-10 Exons Or Characterization Of A Dynamic Mutation Disorder Triplet Repeat By Southern Blot Analysis) Acads (Acyl-Coa Dehydrogenase C-2 To C-3 Short Chain) (Eg Short Chain Acyl-Coa Dehydrogenase Deficiency) Targeted Sequence Analysis (Eg Exons 5 And 6) Aqp2 (Aquaporin 2 [Collecting Duct]) (Eg Nephrogenic Diabetes Insipidus) Full Gene Sequence Arx (Aristaless Related Homeobox) (Eg X-Linked Lissencephaly With Ambiguous Genitalia X-Linked Intellectual Disability) Full Gene Sequence Avpr2 (Arginine Vasopressin Receptor 2) (Eg Nephrogenic Diabetes Insipidus) Full Gene Sequence Bbs10 (Bardet-Biedl Syndrome 10) (Eg Bardet-Biedl Syndrome) Full Gene Sequence Btd (Biotinidase) (Eg Biotinidase Deficiency) Full Gene Sequence C10orf2 (Chromosome 10 Open Reading Frame 2) (Eg Mitochondrial Dna Depletion Syndrome) Full Gene Sequence Cav3 (Caveolin 3) (Eg Cav3-Related Distal Myopathy Limb-Girdle Muscular Dystrophy Type 1c) Full Gene Sequence Cd40lg (Cd40 Ligand) (Eg X-Linked Hyper Igm Syndrome) Full Gene Sequence Cdkn2a (Cyclin-Dependent Kinase Inhibitor 2a) (Eg Cdkn2a-Related Cutaneous Malignant Melanoma Familial Atypical Mole-Malignant Melanoma Syndrome) Full Gene Sequence Clrn1 (Clarin 1) (Eg Usher Syndrome Type 3) Full Gene Sequence Cox6b1 (Cytochrome C Oxidase Subunit Vib Polypeptide 1) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Cpt2 (Carnitine Palmitoyltransferase 2) (Eg Carnitine Palmitoyltransferase Ii Deficiency) Full Gene Sequence Crx (Cone-Rod Homeobox) (Eg Cone-Rod Dystrophy 2 Leber Congenital Amaurosis) Full Gene Sequence Cyp1b1 (Cytochrome P450 Family 1 Subfamily B Polypeptide 1) (Eg Primary Congenital Glaucoma) Full Gene Sequence Egr2 (Early Growth Response 2) (Eg Charcot-Marie-Tooth) Full Gene Sequence Emd (Emerin) (Eg Emery-Dreifuss Muscular Dystrophy) Duplication Deletion Analysis Epm2a (Epilepsy Progressive Myoclonus Type 2a Lafora Disease [Laforin]) (Eg Progressive Myoclonus Epilepsy) Full Gene Sequence Fgf23 (Fibroblast Growth Factor 23) (Eg Hypophosphatemic Rickets) Full Gene Sequence Fgfr2 (Fibroblast Growth Factor Receptor 2) (Eg Craniosynostosis Apert Syndrome Crouzon Syndrome) Targeted Sequence Analysis (Eg Exons 8 10) Fgfr3 (Fibroblast Growth Factor Receptor 3) (Eg Achondroplasia Hypochondroplasia) Targeted Sequence Analysis (Eg Exons 8 11 12 13) Fhl1 (Four And A Half Lim Domains 1) (Eg Emery-Dreifuss Muscular Dystrophy) Full Gene Sequence Fkrp (Fukutin Related Protein) (Eg Congenital Muscular Dystrophy Type 1c [Mdc1c] Limb-Girdle Muscular Dystrophy [Lgmd] Type 2i) Full Gene Sequence Foxg1 (Forkhead Box G1) (Eg Rett Syndrome) Full Gene Sequence Fshmd1a (Facioscapulohumeral Muscular Dystrophy 1a) (Eg Facioscapulohumeral Muscular Dystrophy) Evaluation To Detect Abnormal (Eg Deleted) Alleles Fshmd1a (Facioscapulohumeral Muscular Dystrophy 1a) (Eg Facioscapulohumeral Muscular Dystrophy) Characterization Of Haplotype(S) (Ie Chromosome 4a And 4b Haplotypes) Gh1 (Growth Hormone 1) (Eg Growth Hormone Deficiency) Full Gene Sequence Gp1bb (Glycoprotein Ib [Platelet] Beta Polypeptide) (Eg Bernard-Soulier Syndrome Type B) Full Gene Sequence (For Common Deletion Variants Of Alpha Globin 1 And Alpha Globin 2 Genes Use 81257) Hnf1b (Hnf1 Homeobox B) (Eg Maturity-Onset Diabetes Of The Young [Mody]) Duplication Deletion Analysis Hras (V-Ha-Ras Harvey Rat Sarcoma Viral Oncogene Homolog) (Eg Costello Syndrome) Full Gene Sequence Hsd3b2 (Hydroxy-Delta-5-Steroid Dehydrogenase 3 Beta- And Steroid Delta-Isomerase 2) (Eg 3-Beta-Hydroxysteroid Dehydrogenase Type Ii Deficiency) Full Gene Sequence Hsd11b2 (Hydroxysteroid [11-Beta] Dehydrogenase 2) (Eg Mineralocorticoid Excess Syndrome) Full Gene Sequence Hspb1 (Heat Shock 27kda Protein 1) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Ins (Insulin) (Eg Diabetes Mellitus) Full Gene Sequence Kcnj1 (Potassium Inwardly-Rectifying Channel Subfamily J Member 1) (Eg Bartter Syndrome) Full Gene Sequence Kcnj10 (Potassium Inwardly-Rectifying Channel Subfamily J Member 10) (Eg Sesame Syndrome East Syndrome Sensorineural Hearing Loss) Full Gene Sequence Litaf (Lipopolysaccharide-Induced Tnf Factor) (Eg Charcot-Marie-Tooth) Full Gene Sequence Mefv (Mediterranean Fever) (Eg Familial Mediterranean Fever) Full Gene Sequence Men1 (Multiple Endocrine Neoplasia I) (Eg Multiple Endocrine Neoplasia Type 1 Wermer Syndrome) Duplication Deletion Analysis Mmachc (Methylmalonic Aciduria [Cobalamin Deficiency] Cblc Type With Homocystinuria) (Eg Methylmalonic Acidemia And Homocystinuria) Full Gene Sequence Mpv17 (Mpv17 Mitochondrial Inner Membrane Protein) (Eg Mitochondrial Dna Depletion Syndrome) Duplication Deletion Analysis Ndp (Norrie Disease [Pseudoglioma]) (Eg Norrie Disease) Full Gene Sequence Ndufa1 (Nadh Dehydrogenase [Ubiquinone] 1 Alpha Subcomplex 1 7.5kda) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Ndufaf2 (Nadh Dehydrogenase [Ubiquinone] 1 Alpha Subcomplex Assembly Factor 2) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Ndufs4 (Nadh Dehydrogenase [Ubiquinone] Fe-S Protein 4 18kda [Nadh-Coenzyme Q Reductase]) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Nipa1 (Non-Imprinted In Prader-Willi Angelman Syndrome 1) (Eg Spastic Paraplegia) Full Gene Sequence Nlgn4x (Neuroligin 4 X-Linked) (Eg Autism Spectrum Disorders) Duplication Deletion Analysis Npc2 (Niemann-Pick Disease Type C2 [Epididymal Secretory Protein E1]) (Eg Niemann-Pick Disease Type C2) Full Gene Sequence Nr0b1 (Nuclear Receptor Subfamily 0 Group B Member 1) (Eg Congenital Adrenal Hypoplasia) Full Gene Sequence Pdx1 (Pancreatic And Duodenal Homeobox 1) (Eg Maturity-Onset Diabetes Of The Young [Mody]) Full Gene Sequence Phox2b (Paired-Like Homeobox 2b) (Eg Congenital Central Hypoventilation Syndrome) Full Gene Sequence Plp1 (Proteolipid Protein 1) (Eg Pelizaeus-Merzbacher Disease Spastic Paraplegia) Duplication Deletion Analysis Pqbp1 (Polyglutamine Binding Protein 1) (Eg Renpenning Syndrome) Duplication Deletion Analysis Prnp (Prion Protein) (Eg Genetic Prion Disease) Full Gene Sequence Prop1 (Prop Paired-Like Homeobox 1) (Eg Combined Pituitary Hormone Deficiency) Full Gene Sequence Prph2 (Peripherin 2 [Retinal Degeneration Slow]) (Eg Retinitis Pigmentosa) Full Gene Sequence Prss1 (Protease Serine 1 [Trypsin 1]) (Eg Hereditary Pancreatitis) Full Gene Sequence Raf1 (V-Raf-1 Murine Leukemia Viral Oncogene Homolog 1) (Eg Leopard Syndrome) Targeted Sequence Analysis (Eg Exons 7 12 14 17) Ret (Ret Proto-Oncogene) (Eg Multiple Endocrine Neoplasia Type 2b And Familial Medullary Thyroid Carcinoma) Common Variants (Eg M918t 2647 2648delinstt A883f) Rho (Rhodopsin) (Eg Retinitis Pigmentosa) Full Gene Sequence Rp1 (Retinitis Pigmentosa 1) (Eg Retinitis Pigmentosa) Full Gene Sequence Scn1b (Sodium Channel Voltage-Gated Type I Beta) (Eg Brugada Syndrome) Full Gene Sequence Sco2 (Sco Cytochrome Oxidase Deficient Homolog 2 [Sco1l]) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Sdhc (Succinate Dehydrogenase Complex Subunit C Integral Membrane Protein 15kda) (Eg Hereditary Paraganglioma-Pheochromocytoma Syndrome) Duplication Deletion Analysis Sdhd (Succinate Dehydrogenase Complex Subunit D Integral Membrane Protein) (Eg Hereditary Paraganglioma) Full Gene Sequence Sgcg (Sarcoglycan Gamma [35kda Dystrophin-Associated Glycoprotein]) (Eg Limb-Girdle Muscular Dystrophy) Duplication Deletion Analysis Sh2d1a (Sh2 Domain Containing 1a) (Eg X-Linked Lymphoproliferative Syndrome) Full Gene Sequence Slc16a2 (Solute Carrier Family 16 Member 2 [Thyroid Hormone Transporter]) (Eg Specific Thyroid Hormone Cell Transporter Deficiency Allan-Herndon-Dudley Syndrome) Duplication Deletion Analysis Slc25a20 (Solute Carrier Family 25 [Carnitine Acylcarnitine Translocase] Member 20) (Eg Carnitine-Acylcarnitine Translocase Deficiency) Duplication Deletion Analysis Slc25a4 (Solute Carrier Family 25 [Mitochondrial Carrier Adenine Nucleotide Translocator] Member 4) (Eg Progressive External Ophthalmoplegia) Full Gene Sequence Sod1 (Superoxide Dismutase 1 Soluble) (Eg Amyotrophic Lateral Sclerosis) Full Gene Sequence Spink1 (Serine Peptidase Inhibitor Kazal Type 1) (Eg Hereditary Pancreatitis) Full Gene Sequence Stk11 (Serine Threonine Kinase 11) (Eg Peutz-Jeghers Syndrome) Duplication Deletion Analysis Taco1 (Translational Activator Of Mitochondrial Encoded Cytochrome C Oxidase I) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Thap1 (Thap Domain Containing Apoptosis Associated Protein 1) (Eg Torsion Dystonia) Full Gene Sequence Tor1a (Torsin Family 1 Member A [Torsin A]) (Eg Torsion Dystonia) Full Gene Sequence Ttpa (Tocopherol [Alpha] Transfer Protein) (Eg Ataxia) Full Gene Sequence Ttr (Transthyretin) (Eg Familial Transthyretin Amyloidosis) Full Gene Sequence Twist1 (Twist Homolog 1 [Drosophila]) (Eg Saethre-Chotzen Syndrome) Full Gene Sequence Tyr (Tyrosinase [Oculocutaneous Albinism Ia]) (Eg Oculocutaneous Albinism Ia) Full Gene Sequence Ugt1a1 (Udp Glucuronosyltransferase 1 Family Polypeptide A1) (Eg Hereditary Unconjugated Hyperbilirubinemia [Crigler-Najjar Syndrome]) Full Gene Sequence Ush1g (Usher Syndrome 1g [Autosomal Recessive]) (Eg Usher Syndrome Type 1) Full Gene Sequence Vhl (Von Hippel-Lindau Tumor Suppressor) (Eg Von Hippel-Lindau Familial Cancer Syndrome) Full Gene Sequence Vwf (Von Willebrand Factor) (Eg Von Willebrand Disease Type 1c) Targeted Sequence Analysis (Eg Exons 26 27 37) Zeb2 (Zinc Finger E-Box Binding Homeobox 2) (Eg Mowat-Wilson Syndrome) Duplication Deletion Analysis Znf41 (Zinc Finger Protein 41) (Eg X-Linked Intellectual Disability 89) Full Gene Sequence |
| 81405-CPT | Moderate | Mopath Procedure Level 6, Molecular Pathology Procedure Level 6 (Eg Analysis Of 6-10 Exons By Dna Sequence Analysis Mutation Scanning Or Duplication Deletion Variants Of 11-25 Exons Regionally Targeted Cytogenomic Array Analysis) Abcd1 (Atp-Binding Cassette Sub-Family D [Ald] Member 1) (Eg Adrenoleukodystrophy) Full Gene Sequence Acads (Acyl-Coa Dehydrogenase C-2 To C-3 Short Chain) (Eg Short Chain Acyl-Coa Dehydrogenase Deficiency) Full Gene Sequence Acta2 (Actin Alpha 2 Smooth Muscle Aorta) (Eg Thoracic Aortic Aneurysms And Aortic Dissections) Full Gene Sequence Actc1 (Actin Alpha Cardiac Muscle 1) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Ankrd1 (Ankyrin Repeat Domain 1) (Eg Dilated Cardiomyopathy) Full Gene Sequence Aptx (Aprataxin) (Eg Ataxia With Oculomotor Apraxia 1) Full Gene Sequence Arsa (Arylsulfatase A) (Eg Arylsulfatase A Deficiency) Full Gene Sequence Bckdha (Branched Chain Keto Acid Dehydrogenase E1 Alpha Polypeptide) (Eg Maple Syrup Urine Disease Type 1a) Full Gene Sequence Bcs1l (Bcs1-Like [S. Cerevisiae]) (Eg Leigh Syndrome Mitochondrial Complex Iii Deficiency Gracile Syndrome) Full Gene Sequence Bmpr2 (Bone Morphogenetic Protein Receptor Type Ii [Serine Threonine Kinase]) (Eg Heritable Pulmonary Arterial Hypertension) Duplication Deletion Analysis Casq2 (Calsequestrin 2 [Cardiac Muscle]) (Eg Catecholaminergic Polymorphic Ventricular Tachycardia) Full Gene Sequence Casr (Calcium-Sensing Receptor) (Eg Hypocalcemia) Full Gene Sequence Cdkl5 (Cyclin-Dependent Kinase-Like 5) (Eg Early Infantile Epileptic Encephalopathy) Duplication Deletion Analysis Chrna4 (Cholinergic Receptor Nicotinic Alpha 4) (Eg Nocturnal Frontal Lobe Epilepsy) Full Gene Sequence Chrnb2 (Cholinergic Receptor Nicotinic Beta 2 [Neuronal]) (Eg Nocturnal Frontal Lobe Epilepsy) Full Gene Sequence Cox10 (Cox10 Homolog Cytochrome C Oxidase Assembly Protein) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Cox15 (Cox15 Homolog Cytochrome C Oxidase Assembly Protein) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Cpox (Coproporphyrinogen Oxidase) (Eg Hereditary Coproporphyria) Full Gene Sequence Ctrc (Chymotrypsin C) (Eg Hereditary Pancreatitis) Full Gene Sequence Cyp11b1 (Cytochrome P450 Family 11 Subfamily B Polypeptide 1) (Eg Congenital Adrenal Hyperplasia) Full Gene Sequence Cyp17a1 (Cytochrome P450 Family 17 Subfamily A Polypeptide 1) (Eg Congenital Adrenal Hyperplasia) Full Gene Sequence Cyp21a2 (Cytochrome P450 Family 21 Subfamily A Polypeptide2) (Eg Steroid 21-Hydroxylase Isoform Congenital Adrenal Hyperplasia) Full Gene Sequence Cytogenomic Constitutional Targeted Microarray Analysis Of Chromosome 22q13 By Interrogation Of Genomic Regions For Copy Number And Single Nucleotide Polymorphism (Snp) Variants For Chromosomal Abnormalities (When Performing Cytogenomic [Genome-Wide] Analysis For Constitutional Chromosomal Abnormalities See 81228 81229 81349) (Do Not Report Analyte-Specific Molecular Pathology Procedures Separately When The Specific Analytes Are Included As Part Of The Microarray Analysis Of Chromosome 22q13) (Do Not Report 88271 When Performing Cytogenomic Microarray Analysis) Dbt (Dihydrolipoamide Branched Chain Transacylase E2) (Eg Maple Syrup Urine Disease Type 2) Duplication Deletion Analysis Dcx (Doublecortin) (Eg X-Linked Lissencephaly) Full Gene Sequence Des (Desmin) (Eg Myofibrillar Myopathy) Full Gene Sequence Dfnb59 (Deafness Autosomal Recessive 59) (Eg Autosomal Recessive Nonsyndromic Hearing Impairment) Full Gene Sequence Dguok (Deoxyguanosine Kinase) (Eg Hepatocerebral Mitochondrial Dna Depletion Syndrome) Full Gene Sequence Dhcr7 (7-Dehydrocholesterol Reductase) (Eg Smith-Lemli-Opitz Syndrome) Full Gene Sequence Eif2b2 (Eukaryotic Translation Initiation Factor 2b Subunit 2 Beta 39kda) (Eg Leukoencephalopathy With Vanishing White Matter) Full Gene Sequence Emd (Emerin) (Eg Emery-Dreifuss Muscular Dystrophy) Full Gene Sequence Eng (Endoglin) (Eg Hereditary Hemorrhagic Telangiectasia Type 1) Duplication Deletion Analysis Eya1 (Eyes Absent Homolog 1 [Drosophila]) (Eg Branchio-Oto-Renal [Bor] Spectrum Disorders) Duplication Deletion Analysis Fgfr1 (Fibroblast Growth Factor Receptor 1) (Eg Kallmann Syndrome 2) Full Gene Sequence Fh (Fumarate Hydratase) (Eg Fumarate Hydratase Deficiency Hereditary Leiomyomatosis With Renal Cell Cancer) Full Gene Sequence Fktn (Fukutin) (Eg Limb-Girdle Muscular Dystrophy [Lgmd] Type 2m Or 2l) Full Gene Sequence Ftsj1 (Ftsj Rna 2-O-Methyltransferase 1) (Eg X-Linked Intellectual Disability 9) Duplication Deletion Analysis Gabrg2 (Gamma-Aminobutyric Acid [Gaba] A Receptor Gamma 2) (Eg Generalized Epilepsy With Febrile Seizures) Full Gene Sequence Gch1 (Gtp Cyclohydrolase 1) (Eg Autosomal Dominant Dopa-Responsive Dystonia) Full Gene Sequence Gdap1 (Ganglioside-Induced Differentiation-Associated Protein 1) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Gfap (Glial Fibrillary Acidic Protein) (Eg Alexander Disease) Full Gene Sequence Ghr (Growth Hormone Receptor) (Eg Laron Syndrome) Full Gene Sequence Ghrhr (Growth Hormone Releasing Hormone Receptor) (Eg Growth Hormone Deficiency) Full Gene Sequence Gla (Galactosidase Alpha) (Eg Fabry Disease) Full Gene Sequence Hnf1a (Hnf1 Homeobox A) (Eg Maturity-Onset Diabetes Of The Young [Mody]) Full Gene Sequence Hnf1b (Hnf1 Homeobox B) (Eg Maturity-Onset Diabetes Of The Young [Mody]) Full Gene Sequence Htra1 (Htra Serine Peptidase 1) (Eg Macular Degeneration) Full Gene Sequence Ids (Iduronate 2-Sulfatase) (Eg Mucopolysacchridosis Type Ii) Full Gene Sequence Il2rg (Interleukin 2 Receptor Gamma) (Eg X-Linked Severe Combined Immunodeficiency) Full Gene Sequence Ispd (Isoprenoid Synthase Domain Containing) (Eg Muscle-Eye-Brain Disease Walker-Warburg Syndrome) Full Gene Sequence Kras (Kirsten Rat Sarcoma Viral Oncogene Homolog) (Eg Noonan Syndrome) Full Gene Sequence Lamp2 (Lysosomal-Associated Membrane Protein 2) (Eg Danon Disease) Full Gene Sequence Ldlr (Low Density Lipoprotein Receptor) (Eg Familial Hypercholesterolemia) Duplication Deletion Analysis Men1 (Multiple Endocrine Neoplasia I) (Eg Multiple Endocrine Neoplasia Type 1 Wermer Syndrome) Full Gene Sequence Mmaa (Methylmalonic Aciduria [Cobalamine Deficiency] Type A) (Eg Mmaa-Related Methylmalonic Acidemia) Full Gene Sequence Mmab (Methylmalonic Aciduria [Cobalamine Deficiency] Type B) (Eg Mmaa-Related Methylmalonic Acidemia) Full Gene Sequence Mpi (Mannose Phosphate Isomerase) (Eg Congenital Disorder Of Glycosylation 1b) Full Gene Sequence Mpv17 (Mpv17 Mitochondrial Inner Membrane Protein) (Eg Mitochondrial Dna Depletion Syndrome) Full Gene Sequence Mpz (Myelin Protein Zero) (Eg Charcot-Marie-Tooth) Full Gene Sequence Mtm1 (Myotubularin 1) (Eg X-Linked Centronuclear Myopathy) Duplication Deletion Analysis Myl2 (Myosin Light Chain 2 Regulatory Cardiac Slow) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Myl3 (Myosin Light Chain 3 Alkali Ventricular Skeletal Slow) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Myot (Myotilin) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Ndufs7 (Nadh Dehydrogenase [Ubiquinone] Fe-S Protein 7 20kda [Nadh-Coenzyme Q Reductase]) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Ndufs8 (Nadh Dehydrogenase [Ubiquinone] Fe-S Protein 8 23kda [Nadh-Coenzyme Q Reductase]) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Ndufv1 (Nadh Dehydrogenase [Ubiquinone] Flavoprotein 1 51kda) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Nefl (Neurofilament Light Polypeptide) (Eg Charcot-Marie-Tooth) Full Gene Sequence Nf2 (Neurofibromin 2 [Merlin]) (Eg Neurofibromatosis Type 2) Duplication Deletion Analysis Nlgn3 (Neuroligin 3) (Eg Autism Spectrum Disorders) Full Gene Sequence Nlgn4x (Neuroligin 4 X-Linked) (Eg Autism Spectrum Disorders) Full Gene Sequence Nphp1 (Nephronophthisis 1 [Juvenile]) (Eg Joubert Syndrome) Deletion Analysis And Duplication Analysis If Performed Nphs2 (Nephrosis 2 Idiopathic Steroid-Resistant [Podocin]) (Eg Steroid-Resistant Nephrotic Syndrome) Full Gene Sequence Nsd1 (Nuclear Receptor Binding Set Domain Protein 1) (Eg Sotos Syndrome) Duplication Deletion Analysis Otc (Ornithine Carbamoyltransferase) (Eg Ornithine Transcarbamylase Deficiency) Full Gene Sequence Pafah1b1 (Platelet-Activating Factor Acetylhydrolase 1b Regulatory Subunit 1 [45kda]) (Eg Lissencephaly Miller-Dieker Syndrome) Duplication Deletion Analysis Park2 (Parkinson Protein 2 E3 Ubiquitin Protein Ligase [Parkin]) (Eg Parkinson Disease) Duplication Deletion Analysis Pcca (Propionyl Coa Carboxylase Alpha Polypeptide) (Eg Propionic Acidemia Type 1) Duplication Deletion Analysis Pcdh19 (Protocadherin 19) (Eg Epileptic Encephalopathy) Full Gene Sequence Pdha1 (Pyruvate Dehydrogenase [Lipoamide] Alpha 1) (Eg Lactic Acidosis) Duplication Deletion Analysis Pdhb (Pyruvate Dehydrogenase [Lipoamide] Beta) (Eg Lactic Acidosis) Full Gene Sequence Pink1 (Pten Induced Putative Kinase 1) (Eg Parkinson Disease) Full Gene Sequence Pklr (Pyruvate Kinase Liver And Rbc) (Eg Pyruvate Kinase Deficiency) Full Gene Sequence Plp1 (Proteolipid Protein 1) (Eg Pelizaeus-Merzbacher Disease Spastic Paraplegia) Full Gene Sequence Pou1f1 (Pou Class 1 Homeobox 1) (Eg Combined Pituitary Hormone Deficiency) Full Gene Sequence Prx (Periaxin) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Pqbp1 (Polyglutamine Binding Protein 1) (Eg Renpenning Syndrome) Full Gene Sequence Psen1 (Presenilin 1) (Eg Alzheimer Disease) Full Gene Sequence Rab7a (Rab7a Member Ras Oncogene Family) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Rai1 (Retinoic Acid Induced 1) (Eg Smith-Magenis Syndrome) Full Gene Sequence Reep1 (Receptor Accessory Protein 1) (Eg Spastic Paraplegia) Full Gene Sequence Ret (Ret Proto-Oncogene) (Eg Multiple Endocrine Neoplasia Type 2a And Familial Medullary Thyroid Carcinoma) Targeted Sequence Analysis (Eg Exons 10 11 13-16) Rps19 (Ribosomal Protein S19) (Eg Diamond-Blackfan Anemia) Full Gene Sequence Rrm2b (Ribonucleotide Reductase M2 B [Tp53 Inducible]) (Eg Mitochondrial Dna Depletion) Full Gene Sequence Sco1 (Sco Cytochrome Oxidase Deficient Homolog 1) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Sdhb (Succinate Dehydrogenase Complex Subunit B Iron Sulfur) (Eg Hereditary Paraganglioma) Full Gene Sequence Sdhc (Succinate Dehydrogenase Complex Subunit C Integral Membrane Protein 15kda) (Eg Hereditary Paraganglioma-Pheochromocytoma Syndrome) Full Gene Sequence Sgca (Sarcoglycan Alpha [50kda Dystrophin-Associated Glycoprotein]) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Sgcb (Sarcoglycan Beta [43kda Dystrophin-Associated Glycoprotein]) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Sgcd (Sarcoglycan Delta [35kda Dystrophin-Associated Glycoprotein]) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Sgce (Sarcoglycan Epsilon) (Eg Myoclonic Dystonia) Duplication Deletion Analysis Sgcg (Sarcoglycan Gamma [35kda Dystrophin-Associated Glycoprotein]) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Shoc2 (Soc-2 Suppressor Of Clear Homolog) (Eg Noonan-Like Syndrome With Loose Anagen Hair) Full Gene Sequence Shox (Short Stature Homeobox) (Eg Langer Mesomelic Dysplasia) Full Gene Sequence Sil1 (Sil1 Homolog Endoplasmic Reticulum Chaperone [S. Cerevisiae]) (Eg Ataxia) Full Gene Sequence Slc2a1 (Solute Carrier Family 2 [Facilitated Glucose Transporter] Member 1) (Eg Glucose Transporter Type 1 [Glut 1] Deficiency Syndrome) Full Gene Sequence Slc16a2 (Solute Carrier Family 16 Member 2 [Thyroid Hormone Transporter]) (Eg Specific Thyroid Hormone Cell Transporter Deficiency Allan-Herndon-Dudley Syndrome) Full Gene Sequence Slc22a5 (Solute Carrier Family 22 [Organic Cation Carnitine Transporter] Member 5) (Eg Systemic Primary Carnitine Deficiency) Full Gene Sequence Slc25a20 (Solute Carrier Family 25 [Carnitine Acylcarnitine Translocase] Member 20) (Eg Carnitine-Acylcarnitine Translocase Deficiency) Full Gene Sequence Smad4 (Smad Family Member 4) (Eg Hemorrhagic Telangiectasia Syndrome Juvenile Polyposis) Duplication Deletion Analysis Spast (Spastin) (Eg Spastic Paraplegia) Duplication Deletion Analysis Spg7 (Spastic Paraplegia 7 [Pure And Complicated Autosomal Recessive]) (Eg Spastic Paraplegia) Duplication Deletion Analysis Spred1 (Sprouty-Related Evh1 Domain Containing 1) (Eg Legius Syndrome) Full Gene Sequence Stat3 (Signal Transducer And Activator Of Transcription 3 [Acute-Phase Response Factor]) (Eg Autosomal Dominant Hyper-Ige Syndrome) Targeted Sequence Analysis (Eg Exons 12 13 14 16 17 20 21) Stk11 (Serine Threonine Kinase 11) (Eg Peutz-Jeghers Syndrome) Full Gene Sequence Surf1 (Surfeit 1) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Tardbp (Tar Dna Binding Protein) (Eg Amyotrophic Lateral Sclerosis) Full Gene Sequence Tbx5 (T-Box 5) (Eg Holt-Oram Syndrome) Full Gene Sequence Tcf4 (Transcription Factor 4) (Eg Pitt-Hopkins Syndrome) Duplication Deletion Analysis Tgfbr1 (Transforming Growth Factor Beta Receptor 1) (Eg Marfan Syndrome) Full Gene Sequence Tgfbr2 (Transforming Growth Factor Beta Receptor 2) (Eg Marfan Syndrome) Full Gene Sequence Thrb (Thyroid Hormone Receptor Beta) (Eg Thyroid Hormone Resistance Thyroid Hormone Beta Receptor Deficiency) Full Gene Sequence Or Targeted Sequence Analysis Of >5 Exons Tk2 (Thymidine Kinase 2 Mitochondrial) (Eg Mitochondrial Dna Depletion Syndrome) Full Gene Sequence Tnnc1 (Troponin C Type 1 [Slow]) (Eg Hypertrophic Cardiomyopathy Or Dilated Cardiomyopathy) Full Gene Sequence Tnni3 (Troponin I Type 3 [Cardiac]) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Tpm1 (Tropomyosin 1 [Alpha]) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Tsc1 (Tuberous Sclerosis 1) (Eg Tuberous Sclerosis) Duplication Deletion Analysis Tymp (Thymidine Phosphorylase) (Eg Mitochondrial Dna Depletion Syndrome) Full Gene Sequence Vwf (Von Willebrand Factor) (Eg Von Willebrand Disease Type 2n) Targeted Sequence Analysis (Eg Exons 18-20 23-25) Wt1 (Wilms Tumor 1) (Eg Denys-Drash Syndrome Familial Wilms Tumor) Full Gene Sequence Zeb2 (Zinc Finger E-Box Binding Homeobox 2) (Eg Mowat-Wilson Syndrome) Full Gene Sequence |
| 81406-CPT | Moderate | Mopath Procedure Level 7, Molecular Pathology Procedure Level 7 (Eg Analysis Of 11-25 Exons By Dna Sequence Analysis Mutation Scanning Or Duplication Deletion Variants Of 26-50 Exons) Acadvl (Acyl-Coa Dehydrogenase Very Long Chain) (Eg Very Long Chain Acyl-Coenzyme A Dehydrogenase Deficiency) Full Gene Sequence Actn4 (Actinin Alpha 4) (Eg Focal Segmental Glomerulosclerosis) Full Gene Sequence Afg3l2 (Afg3 Atpase Family Gene 3-Like 2 [S. Cerevisiae]) (Eg Spinocerebellar Ataxia) Full Gene Sequence Aire (Autoimmune Regulator) (Eg Autoimmune Polyendocrinopathy Syndrome Type 1) Full Gene Sequence Aldh7a1 (Aldehyde Dehydrogenase 7 Family Member A1) (Eg Pyridoxine-Dependent Epilepsy) Full Gene Sequence Ano5 (Anoctamin 5) (Eg Limb-Girdle Muscular Dystrophy) Full Gene Sequence Anos1 (Anosmin-1) (Eg Kallmann Syndrome 1) Full Gene Sequence App (Amyloid Beta [A4] Precursor Protein) (Eg Alzheimer Disease) Full Gene Sequence Ass1 (Argininosuccinate Synthase 1) (Eg Citrullinemia Type I) Full Gene Sequence Atl1 (Atlastin Gtpase 1) (Eg Spastic Paraplegia) Full Gene Sequence Atp1a2 (Atpase Na+ K+ Transporting Alpha 2 Polypeptide) (Eg Familial Hemiplegic Migraine) Full Gene Sequence Atp7b (Atpase Cu++ Transporting Beta Polypeptide) (Eg Wilson Disease) Full Gene Sequence Bbs1 (Bardet-Biedl Syndrome 1) (Eg Bardet-Biedl Syndrome) Full Gene Sequence Bbs2 (Bardet-Biedl Syndrome 2) (Eg Bardet-Biedl Syndrome) Full Gene Sequence Bckdhb (Branched-Chain Keto Acid Dehydrogenase E1 Beta Polypeptide) (Eg Maple Syrup Urine Disease Type 1b) Full Gene Sequence Best1 (Bestrophin 1) (Eg Vitelliform Macular Dystrophy) Full Gene Sequence Bmpr2 (Bone Morphogenetic Protein Receptor Type Ii [Serine Threonine Kinase]) (Eg Heritable Pulmonary Arterial Hypertension) Full Gene Sequence Braf (B-Raf Proto-Oncogene Serine Threonine Kinase) (Eg Noonan Syndrome) Full Gene Sequence Bscl2 (Berardinelli-Seip Congenital Lipodystrophy 2 [Seipin]) (Eg Berardinelli-Seip Congenital Lipodystrophy) Full Gene Sequence Btk (Bruton Agammaglobulinemia Tyrosine Kinase) (Eg X-Linked Agammaglobulinemia) Full Gene Sequence Cacnb2 (Calcium Channel Voltage-Dependent Beta 2 Subunit) (Eg Brugada Syndrome) Full Gene Sequence Capn3 (Calpain 3) (Eg Limb-Girdle Muscular Dystrophy [Lgmd] Type 2a Calpainopathy) Full Gene Sequence Cbs (Cystathionine-Beta-Synthase) (Eg Homocystinuria Cystathionine Beta-Synthase Deficiency) Full Gene Sequence Cdh1 (Cadherin 1 Type 1 E-Cadherin [Epithelial]) (Eg Hereditary Diffuse Gastric Cancer) Full Gene Sequence Cdkl5 (Cyclin-Dependent Kinase-Like 5) (Eg Early Infantile Epileptic Encephalopathy) Full Gene Sequence Clcn1 (Chloride Channel 1 Skeletal Muscle) (Eg Myotonia Congenita) Full Gene Sequence Clcnkb (Chloride Channel Voltage-Sensitive Kb) (Eg Bartter Syndrome 3 And 4b) Full Gene Sequence Cntnap2 (Contactin-Associated Protein-Like 2) (Eg Pitt-Hopkins-Like Syndrome 1) Full Gene Sequence Col6a2 (Collagen Type Vi Alpha 2) (Eg Collagen Type Vi-Related Disorders) Duplication Deletion Analysis Cpt1a (Carnitine Palmitoyltransferase 1a [Liver]) (Eg Carnitine Palmitoyltransferase 1a [Cpt1a] Deficiency) Full Gene Sequence Crb1 (Crumbs Homolog 1 [Drosophila]) (Eg Leber Congenital Amaurosis) Full Gene Sequence Crebbp (Creb Binding Protein) (Eg Rubinstein-Taybi Syndrome) Duplication Deletion Analysis Dbt (Dihydrolipoamide Branched Chain Transacylase E2) (Eg Maple Syrup Urine Disease Type 2) Full Gene Sequence Dlat (Dihydrolipoamide S-Acetyltransferase) (Eg Pyruvate Dehydrogenase E2 Deficiency) Full Gene Sequence Dld (Dihydrolipoamide Dehydrogenase) (Eg Maple Syrup Urine Disease Type Iii) Full Gene Sequence Dsc2 (Desmocollin) (Eg Arrhythmogenic Right Ventricular Dysplasia Cardiomyopathy 11) Full Gene Sequence Dsg2 (Desmoglein 2) (Eg Arrhythmogenic Right Ventricular Dysplasia Cardiomyopathy 10) Full Gene Sequence Dsp (Desmoplakin) (Eg Arrhythmogenic Right Ventricular Dysplasia Cardiomyopathy 8) Full Gene Sequence Efhc1 (Ef-Hand Domain [C-Terminal] Containing 1) (Eg Juvenile Myoclonic Epilepsy) Full Gene Sequence Eif2b3 (Eukaryotic Translation Initiation Factor 2b Subunit 3 Gamma 58kda) (Eg Leukoencephalopathy With Vanishing White Matter) Full Gene Sequence Eif2b4 (Eukaryotic Translation Initiation Factor 2b Subunit 4 Delta 67kda) (Eg Leukoencephalopathy With Vanishing White Matter) Full Gene Sequence Eif2b5 (Eukaryotic Translation Initiation Factor 2b Subunit 5 Epsilon 82kda) (Eg Childhood Ataxia With Central Nervous System Hypomyelination Vanishing White Matter) Full Gene Sequence Eng (Endoglin) (Eg Hereditary Hemorrhagic Telangiectasia Type 1) Full Gene Sequence Eya1 (Eyes Absent Homolog 1 [Drosophila]) (Eg Branchio-Oto-Renal [Bor] Spectrum Disorders) Full Gene Sequence F8 (Coagulation Factor Viii) (Eg Hemophilia A) Duplication Deletion Analysis Fah (Fumarylacetoacetate Hydrolase [Fumarylacetoacetase]) (Eg Tyrosinemia Type 1) Full Gene Sequence Fastkd2 (Fast Kinase Domains 2) (Eg Mitochondrial Respiratory Chain Complex Iv Deficiency) Full Gene Sequence Fig4 (Fig4 Homolog Sac1 Lipid Phosphatase Domain Containing [S. Cerevisiae]) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Ftsj1 (Ftsj Rna 2-O-Methyltransferase 1) (Eg X-Linked Intellectual Disability 9) Full Gene Sequence Fus (Fused In Sarcoma) (Eg Amyotrophic Lateral Sclerosis) Full Gene Sequence Gaa (Glucosidase Alpha Acid) (Eg Glycogen Storage Disease Type Ii [Pompe Disease]) Full Gene Sequence Galc (Galactosylceramidase) (Eg Krabbe Disease) Full Gene Sequence Galt (Galactose-1-Phosphate Uridylyltransferase) (Eg Galactosemia) Full Gene Sequence Gars (Glycyl-Trna Synthetase) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Gcdh (Glutaryl-Coa Dehydrogenase) (Eg Glutaricacidemia Type 1) Full Gene Sequence Gck (Glucokinase [Hexokinase 4]) (Eg Maturity-Onset Diabetes Of The Young [Mody]) Full Gene Sequence Glud1 (Glutamate Dehydrogenase 1) (Eg Familial Hyperinsulinism) Full Gene Sequence Gne (Glucosamine [Udp-N-Acetyl]-2-Epimerase N-Acetylmannosamine Kinase) (Eg Inclusion Body Myopathy 2 [Ibm2] Nonaka Myopathy) Full Gene Sequence Grn (Granulin) (Eg Frontotemporal Dementia) Full Gene Sequence Hadha (Hydroxyacyl-Coa Dehydrogenase 3-Ketoacyl-Coa Thiolase Enoyl-Coa Hydratase [Trifunctional Protein] Alpha Subunit) (Eg Long Chain Acyl-Coenzyme A Dehydrogenase Deficiency) Full Gene Sequence Hadhb (Hydroxyacyl-Coa Dehydrogenase 3-Ketoacyl-Coa Thiolase Enoyl-Coa Hydratase [Trifunctional Protein] Beta Subunit) (Eg Trifunctional Protein Deficiency) Full Gene Sequence Hexa (Hexosaminidase A Alpha Polypeptide) (Eg Tay-Sachs Disease) Full Gene Sequence Hlcs (Hlcs Holocarboxylase Synthetase) (Eg Holocarboxylase Synthetase Deficiency) Full Gene Sequence Hmbs (Hydroxymethylbilane Synthase) (Eg Acute Intermittent Porphyria) Full Gene Sequence Hnf4a (Hepatocyte Nuclear Factor 4 Alpha) (Eg Maturity-Onset Diabetes Of The Young [Mody]) Full Gene Sequence Idua (Iduronidase Alpha-L-) (Eg Mucopolysaccharidosis Type I) Full Gene Sequence Inf2 (Inverted Formin Fh2 And Wh2 Domain Containing) (Eg Focal Segmental Glomerulosclerosis) Full Gene Sequence Ivd (Isovaleryl-Coa Dehydrogenase) (Eg Isovaleric Acidemia) Full Gene Sequence Jag1 (Jagged 1) (Eg Alagille Syndrome) Duplication Deletion Analysis Jup (Junction Plakoglobin) (Eg Arrhythmogenic Right Ventricular Dysplasia Cardiomyopathy 11) Full Gene Sequence Kcnh2 (Potassium Voltage-Gated Channel Subfamily H [Eag-Related] Member 2) (Eg Short Qt Syndrome Long Qt Syndrome) Full Gene Sequence Kcnq1 (Potassium Voltage-Gated Channel Kqt-Like Subfamily Member 1) (Eg Short Qt Syndrome Long Qt Syndrome) Full Gene Sequence Kcnq2 (Potassium Voltage-Gated Channel Kqt-Like Subfamily Member 2) (Eg Epileptic Encephalopathy) Full Gene Sequence Ldb3 (Lim Domain Binding 3) (Eg Familial Dilated Cardiomyopathy Myofibrillar Myopathy) Full Gene Sequence Ldlr (Low Density Lipoprotein Receptor) (Eg Familial Hypercholesterolemia) Full Gene Sequence Lepr (Leptin Receptor) (Eg Obesity With Hypogonadism) Full Gene Sequence Lhcgr (Luteinizing Hormone Choriogonadotropin Receptor) (Eg Precocious Male Puberty) Full Gene Sequence Lmna (Lamin A C) (Eg Emery-Dreifuss Muscular Dystrophy [Edmd1 2 And 3] Limb-Girdle Muscular Dystrophy [Lgmd] Type 1b Dilated Cardiomyopathy [Cmd1a] Familial Partial Lipodystrophy [Fpld2]) Full Gene Sequence Lrp5 (Low Density Lipoprotein Receptor-Related Protein 5) (Eg Osteopetrosis) Full Gene Sequence Map2k1 (Mitogen-Activated Protein Kinase 1) (Eg Cardiofaciocutaneous Syndrome) Full Gene Sequence Map2k2 (Mitogen-Activated Protein Kinase 2) (Eg Cardiofaciocutaneous Syndrome) Full Gene Sequence Mapt (Microtubule-Associated Protein Tau) (Eg Frontotemporal Dementia) Full Gene Sequence Mccc1 (Methylcrotonoyl-Coa Carboxylase 1 [Alpha]) (Eg 3-Methylcrotonyl-Coa Carboxylase Deficiency) Full Gene Sequence Mccc2 (Methylcrotonoyl-Coa Carboxylase 2 [Beta]) (Eg 3-Methylcrotonyl Carboxylase Deficiency) Full Gene Sequence Mfn2 (Mitofusin 2) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Mtm1 (Myotubularin 1) (Eg X-Linked Centronuclear Myopathy) Full Gene Sequence Mut (Methylmalonyl Coa Mutase) (Eg Methylmalonic Acidemia) Full Gene Sequence Mutyh (Muty Homolog [E. Coli]) (Eg Myh-Associated Polyposis) Full Gene Sequence Ndufs1 (Nadh Dehydrogenase [Ubiquinone] Fe-S Protein 1 75kda [Nadh-Coenzyme Q Reductase]) (Eg Leigh Syndrome Mitochondrial Complex I Deficiency) Full Gene Sequence Nf2 (Neurofibromin 2 [Merlin]) (Eg Neurofibromatosis Type 2) Full Gene Sequence Notch3 (Notch 3) (Eg Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy [Cadasil]) Targeted Sequence Analysis (Eg Exons 1-23) Npc1 (Niemann-Pick Disease Type C1) (Eg Niemann-Pick Disease) Full Gene Sequence Nphp1 (Nephronophthisis 1 [Juvenile]) (Eg Joubert Syndrome) Full Gene Sequence Nsd1 (Nuclear Receptor Binding Set Domain Protein 1) (Eg Sotos Syndrome) Full Gene Sequence Opa1 (Optic Atrophy 1) (Eg Optic Atrophy) Duplication Deletion Analysis Optn (Optineurin) (Eg Amyotrophic Lateral Sclerosis) Full Gene Sequence Pafah1b1 (Platelet-Activating Factor Acetylhydrolase 1b Regulatory Subunit 1 [45kda]) (Eg Lissencephaly Miller-Dieker Syndrome) Full Gene Sequence Pah (Phenylalanine Hydroxylase) (Eg Phenylketonuria) Full Gene Sequence Park2 (Parkinson Protein 2 E3 Ubiquitin Protein Ligase [Parkin]) (Eg Parkinson Disease) Full Gene Sequence Pax2 (Paired Box 2) (Eg Renal Coloboma Syndrome) Full Gene Sequence Pc (Pyruvate Carboxylase) (Eg Pyruvate Carboxylase Deficiency) Full Gene Sequence Pcca (Propionyl Coa Carboxylase Alpha Polypeptide) (Eg Propionic Acidemia Type 1) Full Gene Sequence Pccb (Propionyl Coa Carboxylase Beta Polypeptide) (Eg Propionic Acidemia) Full Gene Sequence Pcdh15 (Protocadherin-Related 15) (Eg Usher Syndrome Type 1f) Duplication Deletion Analysis Pcsk9 (Proprotein Convertase Subtilisin Kexin Type 9) (Eg Familial Hypercholesterolemia) Full Gene Sequence Pdha1 (Pyruvate Dehydrogenase [Lipoamide] Alpha 1) (Eg Lactic Acidosis) Full Gene Sequence Pdhx (Pyruvate Dehydrogenase Complex Component X) (Eg Lactic Acidosis) Full Gene Sequence Phex (Phosphate-Regulating Endopeptidase Homolog X-Linked) (Eg Hypophosphatemic Rickets) Full Gene Sequence Pkd2 (Polycystic Kidney Disease 2 [Autosomal Dominant]) (Eg Polycystic Kidney Disease) Full Gene Sequence Pkp2 (Plakophilin 2) (Eg Arrhythmogenic Right Ventricular Dysplasia Cardiomyopathy 9) Full Gene Sequence Pnkd (Paroxysmal Nonkinesigenic Dyskinesia) (Eg Paroxysmal Nonkinesigenic Dyskinesia) Full Gene Sequence Polg (Polymerase [Dna Directed] Gamma) (Eg Alpers-Huttenlocher Syndrome Autosomal Dominant Progressive External Ophthalmoplegia) Full Gene Sequence Pomgnt1 (Protein O-Linked Mannose Beta12-N Acetylglucosaminyltransferase) (Eg Muscle-Eye-Brain Disease Walker-Warburg Syndrome) Full Gene Sequence Pomt1 (Protein-O-Mannosyltransferase 1) (Eg Limb-Girdle Muscular Dystrophy [Lgmd] Type 2k Walker-Warburg Syndrome) Full Gene Sequence Pomt2 (Protein-O-Mannosyltransferase 2) (Eg Limb-Girdle Muscular Dystrophy [Lgmd] Type 2n Walker-Warburg Syndrome) Full Gene Sequence Ppox (Protoporphyrinogen Oxidase) (Eg Variegate Porphyria) Full Gene Sequence Prkag2 (Protein Kinase Amp-Activated Gamma 2 Non-Catalytic Subunit) (Eg Familial Hypertrophic Cardiomyopathy With Wolff-Parkinson-White Syndrome Lethal Congenital Glycogen Storage Disease Of Heart) Full Gene Sequence Prkcg (Protein Kinase C Gamma) (Eg Spinocerebellar Ataxia) Full Gene Sequence Psen2 (Presenilin 2 [Alzheimer Disease 4]) (Eg Alzheimer Disease) Full Gene Sequence Ptpn11 (Protein Tyrosine Phosphatase Non-Receptor Type 11) (Eg Noonan Syndrome Leopard Syndrome) Full Gene Sequence Pygm (Phosphorylase Glycogen Muscle) (Eg Glycogen Storage Disease Type V Mcardle Disease) Full Gene Sequence Raf1 (V-Raf-1 Murine Leukemia Viral Oncogene Homolog 1) (Eg Leopard Syndrome) Full Gene Sequence Ret (Ret Proto-Oncogene) (Eg Hirschsprung Disease) Full Gene Sequence Rpe65 (Retinal Pigment Epithelium-Specific Protein 65kda) (Eg Retinitis Pigmentosa Leber Congenital Amaurosis) Full Gene Sequence Ryr1 (Ryanodine Receptor 1 Skeletal) (Eg Malignant Hyperthermia) Targeted Sequence Analysis Of Exons With Functionally-Confirmed Mutations Scn4a (Sodium Channel Voltage-Gated Type Iv Alpha Subunit) (Eg Hyperkalemic Periodic Paralysis) Full Gene Sequence Scnn1a (Sodium Channel Nonvoltage-Gated 1 Alpha) (Eg Pseudohypoaldosteronism) Full Gene Sequence Scnn1b (Sodium Channel Nonvoltage-Gated 1 Beta) (Eg Liddle Syndrome Pseudohypoaldosteronism) Full Gene Sequence Scnn1g (Sodium Channel Nonvoltage-Gated 1 Gamma) (Eg Liddle Syndrome Pseudohypoaldosteronism) Full Gene Sequence Sdha (Succinate Dehydrogenase Complex Subunit A Flavoprotein [Fp]) (Eg Leigh Syndrome Mitochondrial Complex Ii Deficiency) Full Gene Sequence Setx (Senataxin) (Eg Ataxia) Full Gene Sequence Sgce (Sarcoglycan Epsilon) (Eg Myoclonic Dystonia) Full Gene Sequence Sh3tc2 (Sh3 Domain And Tetratricopeptide Repeats 2) (Eg Charcot-Marie-Tooth Disease) Full Gene Sequence Slc9a6 (Solute Carrier Family 9 [Sodium Hydrogen Exchanger] Member 6) (Eg Christianson Syndrome) Full Gene Sequence Slc26a4 (Solute Carrier Family 26 Member 4) (Eg Pendred Syndrome) Full Gene Sequence Slc37a4 (Solute Carrier Family 37 [Glucose-6-Phosphate Transporter] Member 4) (Eg Glycogen Storage Disease Type Ib) Full Gene Sequence Smad4 (Smad Family Member 4) (Eg Hemorrhagic Telangiectasia Syndrome Juvenile Polyposis) Full Gene Sequence Sos1 (Son Of Sevenless Homolog 1) (Eg Noonan Syndrome Gingival Fibromatosis) Full Gene Sequence Spast (Spastin) (Eg Spastic Paraplegia) Full Gene Sequence Spg7 (Spastic Paraplegia 7 [Pure And Complicated Autosomal Recessive]) (Eg Spastic Paraplegia) Full Gene Sequence Stxbp1 (Syntaxin-Binding Protein 1) (Eg Epileptic Encephalopathy) Full Gene Sequence Taz (Tafazzin) (Eg Methylglutaconic Aciduria Type 2 Barth Syndrome) Full Gene Sequence Tcf4 (Transcription Factor 4) (Eg Pitt-Hopkins Syndrome) Full Gene Sequence Th (Tyrosine Hydroxylase) (Eg Segawa Syndrome) Full Gene Sequence Tmem43 (Transmembrane Protein 43) (Eg Arrhythmogenic Right Ventricular Cardiomyopathy) Full Gene Sequence Tnnt2 (Troponin T Type 2 [Cardiac]) (Eg Familial Hypertrophic Cardiomyopathy) Full Gene Sequence Trpc6 (Transient Receptor Potential Cation Channel Subfamily C Member 6) (Eg Focal Segmental Glomerulosclerosis) Full Gene Sequence Tsc1 (Tuberous Sclerosis 1) (Eg Tuberous Sclerosis) Full Gene Sequence Tsc2 (Tuberous Sclerosis 2) (Eg Tuberous Sclerosis) Duplication Deletion Analysis Ube3a (Ubiquitin Protein Ligase E3a) (Eg Angelman Syndrome) Full Gene Sequence Umod (Uromodulin) (Eg Glomerulocystic Kidney Disease With Hyperuricemia And Isosthenuria) Full Gene Sequence Vwf (Von Willebrand Factor) (Von Willebrand Disease Type 2a) Extended Targeted Sequence Analysis (Eg Exons 11-16 24-26 51 52) Was (Wiskott-Aldrich Syndrome [Eczema-Thrombocytopenia]) (Eg Wiskott-Aldrich Syndrome) Full Gene Sequence |
What is a fee schedule?
A fee schedule is a list of fixed prices that healthcare providers charge for specific services, including CPT 81405. These prices vary depending on payer type (Medicare, Medicaid, private insurance), geographic location, and provider contracts.
Understanding the 81405 fee schedule helps patients estimate costs and providers optimize billing for accurate reimbursements.
Factors that affect fee schedules
Medicare & Medicaid Rates
Government-set reimbursement amounts
Private Insurance Rates
Negotiated rates between providers and insurance companies
Geographic Location
Costs may be higher in urban areas.
Provider Type
Hospital providers may have different rates than private practice.
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