GEN HEKİMİ

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C10ORF2

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

Progressive External Ophthalmoplegia (PEO)/Optic Atrophy Nuclear Gene Panel

C12ORF65

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Hereditary Spastic Paraplegia Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

Progressive External Ophthalmoplegia (PEO)/Optic Atrophy Nuclear Gene Panel

C19ORF12

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

C5ORF42

Comprehensive Brain Malformations Panel

Joubert Syndrome and Related Disorders Panel

Prenatal Joubert Syndrome and Related Disorders Panel

C9ORF72

C9ORF72 Repeat Analysis

CA5A

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

CABP2

Hearing Loss Test

CABP4

CABP4 Gene Sequencing

CACNA1A

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

CACNA1C

Custom Arrhythmia Panel *

Custom Brugada Syndrome (BrS) Panel *

Custom Combined Cardiac Panel *

Custom LQTS Panel *

Custom SQTS Panel *

Arrhythmia Panel

BrS Panel

Combined Cardiac Panel

LQTS Panel

SQTS Panel

CACNA1D

Hearing Loss Test

CACNA1F

CACNA1F Gene Sequencing

CACNA1S

Neuromuscular Disorders Panel

CACNA2D1

Custom Arrhythmia Panel *

Custom Combined Cardiac Panel *

Arrhythmia Panel

Combined Cardiac Panel

CACNB2

Custom Arrhythmia Panel *

Custom Brugada Syndrome (BrS) Panel *

Custom Combined Cardiac Panel *

Custom SQTS Panel *

Arrhythmia Panel

BrS Panel

Combined Cardiac Panel

SQTS Panel

CALM1

Custom Arrhythmia Panel *

Custom Combined Cardiac Panel *

Custom CPVT Panel *

Custom LQTS Panel *

Custom SCA Arrhythmia Panel *

Arrhythmia Panel

Combined Cardiac Panel

CPVT Panel

LQTS Panel

SCA Arrhythmia Panel

CALM2

Custom Arrhythmia Panel *

Custom Combined Cardiac Panel *

Custom CPVT Panel *

Custom LQTS Panel *

Custom SCA Arrhythmia Panel *

Arrhythmia Panel

Combined Cardiac Panel

CPVT Panel

LQTS Panel

SCA Arrhythmia Panel

CALM3

Custom Arrhythmia Panel *

Custom Combined Cardiac Panel *

Custom CPVT Panel *

Custom LQTS Panel *

Custom SCA Arrhythmia Panel *

Arrhythmia Panel

Combined Cardiac Panel

CPVT Panel

LQTS Panel

SCA Arrhythmia Panel

CAPN3

Limb-Girdle Muscular Dystrophy Panel

Neuromuscular Disorders Panel

CARS2

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

CASK

Comprehensive Brain Malformations Panel

Epilepsy Del/Dup Panel

Microcephaly Panel

Pontocerebellar Hypoplasia Panel

Prenatal Pontocerebellar Panel

CASP10

CASP10 Gene Sequencing

CASP14

Congenital Ichthyosis XomeDxSlice

CASP8

CASP8 Gene Sequencing

CASQ2

Custom Arrhythmia Panel *

Custom Combined Cardiac Panel *

Custom CPVT Panel *

Custom SCA Arrhythmia Panel *

Arrhythmia Panel

Combined Cardiac Panel

CPVT Panel

SCA Arrhythmia Panel

CASR

CASR Gene Sequencing

CATSPER2

Hearing Loss Test

CAV1

Pulmonary Arterial Hypertension Panel

CAV3

Custom Arrhythmia Panel *

Custom Cardiomyopathy Panel *

Custom Combined Cardiac Panel *

Custom HCM Panel *

Custom LQTS Panel *

Custom SCA Arrhythmia Panel *

Arrhythmia Panel

Cardiomyopathy Panel

Combined Cardiac Panel

HCM Panel

Limb-Girdle Muscular Dystrophy Panel

LQTS Panel

Neuromuscular Disorders Panel

SCA Arrhythmia Panel

CBL

CBL/NRAS Gene Sequencing

Noonan and RASopathies Panel

CBS

Custom HDCT Panel *

Custom Marfan/TAAD & Related Disorders Panel *

HDCT Panel

CBS Gene Sequencing

Marfan/TAAD Panel

Rest of Marfan/TAAD Sequencing & Del/Dup Panel

CC2D2A

Comprehensive Brain Malformations Panel

Joubert Syndrome and Related Disorders Panel

Prenatal Joubert Syndrome and Related Disorders Panel

CCDC50

Hearing Loss Test

CCM2

CCM Tier 2

CCM2 Gene Sequencing

Cerebral Cavernous Malformations (CCM) Panel

CCND2

Comprehensive Brain Malformations Panel

Cortical Brain Malformations Panel

CD151

Epidermolysis Bullosa (EB) XomeDxSlice

CD164

Hearing Loss Test

CD320

Methylmalonic Acidemia, Cobalamin Metabolism and Related Disorders Sequencing Panel

Reflex Del/Dup Testing After MMA and Related Disorders Panel

CD3D

B-positive SCID Panel

Comprehensive SCID Panel

CD3E

B-positive SCID Panel

Comprehensive SCID Panel

CD3Z

B-positive SCID Panel

Comprehensive SCID Panel

CD40

CD40 Gene Sequencing

CD40LG

CD40LG Gene Sequencing

CDC14A

Hearing Loss Test

CDC73 (HRPT2)

OncoGeneDx Custom Panel

CDC73 (HRPT2) Gene Sequencing

CDC73 (HRPT2) Gene Sequencing and Del/Dup

CDC73 (HRPT2) Remaining Exons Sequencing

CDC73 (HRPT2) Select Exons Sequencing

Pediatric Tumor Panel

CDH1

OncoGeneDx Custom Panel

Breast Cancer High Risk Panel

Breast Cancer High Risk Panel and PALB2

Breast Cancer High/Moderate Risk Panel

Breast/Ovarian Cancer Panel

Colorectal Cancer Panel

Comprehensive Cancer Panel

High/Moderate Risk Panel

CDH23

Hearing Loss Test

Usher Syndrome Del/Dup Panel

Usher Syndrome Panel

CDK4

OncoGeneDx Custom Panel

CDKN2A (p16) & CDK4 (Exon2) Sequencing

Comprehensive Cancer Panel

Familial Cutaneous Malignant Melanoma

Pancreatic Cancer Panel

CDK5RAP2

Microcephaly Panel

CDKL5

CDKL5 Gene Sequencing

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

Microcephaly Panel

Rett/Angelman Syndrome Panel

STAT Epilepsy Panel

CDKN2A

OncoGeneDx Custom Panel

CDKN2A (p16) & CDK4 (Exon2) Sequencing

CDKN2A (p16) Gene Sequencing

Comprehensive Cancer Panel

Familial Cutaneous Malignant Melanoma

High/Moderate Risk Panel

Pancreatic Cancer Panel

CDSN

Epidermolysis Bullosa (EB) XomeDxSlice

CEACAM16

Hearing Loss Test

CENPJ

Microcephaly Panel

CEP152

Microcephaly Panel

CEP290

CEP290 Hot Spots

Comprehensive Brain Malformations Panel

Joubert Syndrome and Related Disorders Panel

LCA Tier 1

Prenatal Joubert Syndrome and Related Disorders Panel

CEP41

Comprehensive Brain Malformations Panel

Joubert Syndrome and Related Disorders Panel

Prenatal Joubert Syndrome and Related Disorders Panel

CERKL

arRP Sequencing Panel

CERKL Gene Sequencing

CERS3

Congenital Ichthyosis XomeDxSlice

CFL2

Congenital Myopathies & Muscular Dystrophies Panel

Neuromuscular Disorders Panel

CHAT

Congenital Myasthenia Syndromes Panel

CHD2

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

CHD7

CHD7 Gene Sequencing

Hypogonadotropic Hypogonadism Gene Sequencing and Del/Dup Panel

Prenatal 46, XY DSD Panel

Prenatal CHD7 Gene Sequencing

CHEK2

OncoGeneDx Custom Panel

Breast Cancer High/Moderate Risk Panel

Breast/Ovarian Cancer Panel

Colorectal Cancer Panel

Comprehensive Cancer Panel

Endometrial Cancer Panel

Hereditary Prostate Cancer Panel

High/Moderate Risk Panel

CHKB

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Congenital Myopathies & Muscular Dystrophies Panel

Neuromuscular Disorders Panel

CHM

CHM Gene Sequencing

CHMP1A

Comprehensive Brain Malformations Panel

Pontocerebellar Hypoplasia Panel

Prenatal Pontocerebellar Panel

CHRM2

Custom Cardiomyopathy Panel *

Custom Combined Cardiac Panel *

Custom DCM/LVNC Panel *

Cardiomyopathy Panel

Combined Cardiac Panel

DCM/LVNC Panel

CHRNA1

Congenital Myasthenia Syndromes Panel

CHRNA2

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

CHRNA4

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

CHRNA7

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

CHRNB1

Congenital Myasthenia Syndromes Panel

CHRNB2

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

CHRND

Congenital Myasthenia Syndromes Panel

CHRNE

Congenital Myasthenia Syndromes Panel

CHST14

Custom HDCT Panel *

HDCT Panel

CHST8

Epidermolysis Bullosa (EB) XomeDxSlice

CIB2

Hearing Loss Test

CISD2

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Progressive External Ophthalmoplegia (PEO)/Optic Atrophy Nuclear Gene Panel

CLCN1

Neuromuscular Disorders Panel

CLCN5

CLCN5 Gene Sequencing

CLDN1

Congenital Ichthyosis XomeDxSlice

CLDN14

Hearing Loss Test

CLIC5

Hearing Loss Test

CLN3

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

Progressive Myoclonic Epilepsy Panel

CLN5

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

Progressive Myoclonic Epilepsy Panel

CLN6

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

Progressive Myoclonic Epilepsy Panel

CLN8

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

Progressive Myoclonic Epilepsy Panel

CLP1

Comprehensive Brain Malformations Panel

Pontocerebellar Hypoplasia Panel

Prenatal Pontocerebellar Panel

CLPB

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Methylglutaconic Aciduria Nuclear Gene Panel

Progressive External Ophthalmoplegia (PEO)/Optic Atrophy Nuclear Gene Panel

CLPP

Hearing Loss Test

CLRN1

Hearing Loss Test

Usher Syndrome Del/Dup Panel

Usher Syndrome Panel

CNBP

CNBP Repeat Analysis

CNGA1

arRP Sequencing Panel

CNGA1 Gene Sequencing

CNGA3

CNGA3 Gene Sequencing

CNGB3

CNGB3 Gene Sequencing

CNTN1

Neuromuscular Disorders Panel

CNTNAP2

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

Rett/Angelman Syndrome Panel

COA5 (C2ORF64)

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

COA6

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

COASY

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

COCH

Hearing Loss Test

COG4

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

COG5

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

COG6

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

COG7

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

COG8

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

COL11A1

Custom HDCT Panel *

HDCT Panel

COL11A2

Custom HDCT Panel *

HDCT Panel

Hearing Loss Test

COL17A1

COL17A1 Gene Sequencing

Epidermolysis Bullosa (EB) XomeDxSlice

COL1A1

Custom HDCT Panel *

HDCT Panel

Osteogenesis Imperfecta Panel

Prenatal Skeletal Dysplasia Panel

COL1A2

Custom HDCT Panel *

HDCT Panel

Osteogenesis Imperfecta Panel

Prenatal Skeletal Dysplasia Panel

COL2A1

Custom HDCT Panel *

HDCT Panel

Achondrogenesis Panel

Prenatal Skeletal Dysplasia Panel

COL3A1

Custom HDCT Panel *

Custom Marfan/TAAD & Related Disorders Panel *

HDCT Panel

Marfan/TAAD Panel

Rest of Marfan/TAAD Sequencing & Del/Dup Panel

COL4A3

Hearing Loss Test

COL4A4

Hearing Loss Test

COL4A5

COL4A5 Gene Sequencing

COL4A6

Hearing Loss Test

COL5A1

Custom HDCT Panel *

Custom Marfan/TAAD & Related Disorders Panel *

HDCT Panel

Marfan/TAAD Panel

Rest of Marfan/TAAD Sequencing & Del/Dup Panel

COL5A2

Custom HDCT Panel *

Custom Marfan/TAAD & Related Disorders Panel *

HDCT Panel

Marfan/TAAD Panel

Rest of Marfan/TAAD Sequencing & Del/Dup Panel

COL6A1

Congenital Myopathies & Muscular Dystrophies Panel

Neuromuscular Disorders Panel

COL6A2

Congenital Myopathies & Muscular Dystrophies Panel

Neuromuscular Disorders Panel

COL6A3

Congenital Myopathies & Muscular Dystrophies Panel

Neuromuscular Disorders Panel

COL7A1

COL7A1 Gene Sequencing

Epidermolysis Bullosa (EB) XomeDxSlice

COL9A1

Custom HDCT Panel *

HDCT Panel

COL9A2

Custom HDCT Panel *

HDCT Panel

COLQ

Congenital Myasthenia Syndromes Panel

COMP

COMP Gene Sequencing

COQ2

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

COQ4

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

COQ6

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

COQ9

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

CORO1A

B-positive SCID Panel

Comprehensive SCID Panel

COX10

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

COX14 (C12ORF62)

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

COX15

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

COX20 (FAM36A)

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

COX4I2

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

COX6A1

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

COX6B1

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

COX7B

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Progressive External Ophthalmoplegia (PEO)/Optic Atrophy Nuclear Gene Panel

CPS1

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Hyperammonemia, Urea Cycle and Transporter Defects Sequencing Panel

Reflex Del/Dup Testing after Hyperammonemia Panel

CPT1A

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

CPT1A Gene Sequencing

Fatty Acid Oxidation Sequencing Panel

Hyperammonemia, Urea Cycle and Transporter Defects Sequencing Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

Reflex Del/Dup Testing After Fatty Acid Oxidation Disorders Panel

Reflex Del/Dup Testing after Hyperammonemia Panel

CPT2

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

CPT2 Gene Sequencing

Fatty Acid Oxidation Sequencing Panel

Hyperammonemia, Urea Cycle and Transporter Defects Sequencing Panel

Metabolic Myopathy

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

Reflex Del/Dup Testing After Fatty Acid Oxidation Disorders Panel

Reflex Del/Dup Testing after Hyperammonemia Panel

Reflex Del/Dup Testing After Metabolic Myopathy

CRB1

arRP Del/Dup Panel

arRP Sequencing Panel

CRB1 Gene Sequencing

LCA Tier 1

LCA Tier 2

CREBBP

CREBBP Remaining Exons Sequencing

CREBBP Select Exons Sequencing & Del/Dup

CREBBP Sequencing & Del/Dup

Epilepsy Del/Dup Panel

CRTAP

Osteogenesis Imperfecta Panel

Prenatal Skeletal Dysplasia Panel

CRX

CRX Gene Sequencing

CRYAB

Custom Cardiomyopathy Panel *

Custom Combined Cardiac Panel *

• CUSTOMIZE

Custom DCM/LVNC Panel *

Cardiomyopathy Panel

Combined Cardiac Panel

DCM/LVNC Panel

Myofibrillar Myopathy Panel

Neuromuscular Disorders Panel

CRYM

Hearing Loss Test

CSPP1

Comprehensive Brain Malformations Panel

Joubert Syndrome and Related Disorders Panel

Prenatal Joubert Syndrome and Related Disorders Panel

CSRP3

Custom Cardiomyopathy Panel *

Custom Combined Cardiac Panel *

Custom DCM/LVNC Panel *

Custom HCM Panel *

Cardiomyopathy Panel

Combined Cardiac Panel

DCM/LVNC Panel

HCM Panel

CSTA

Epidermolysis Bullosa (EB) XomeDxSlice

CSTB

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Progressive Myoclonic Epilepsy Panel

CTSC

CTSC Gene Sequencing

CTSD

Childhood-Onset Epilepsy Panel

Comprehensive Epilepsy Panel

Epilepsy Del/Dup Panel

Infantile Epilepsy Panel

Progressive Myoclonic Epilepsy Panel

CUL4B

Comprehensive Brain Malformations Panel

Cortical Brain Malformations Panel

Syndromic Macrocephaly/Overgrowth Panel

CYBA

CYBA Gene Sequencing

CYBB

CYBB Gene Sequencing

CYC1

Combined Mito Genome Plus Mito Nuclear Gene Panel

Comprehensive Mitochondrial Nuclear Gene Panel

Lactic Acidosis/Pyruvate Metabolism Nuclear Gene Panel

Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene Panel

CYP17A1

CYP17A1 Gene Sequencing

Premature Ovarian Failure Sequencing Panel

CYP19A1

CYP19A1 Gene Sequencing

Premature Ovarian Failure Sequencing Panel

CYP1B1

CYP1B1 Gene Sequencing

CYP27A1

Hereditary Spastic Paraplegia Related Inborn Errors of Metabolism Panel

CYP27B1

CYP27B1 Select Exons Sequencing

CYP2U1

Comprehensive Hereditary Spastic Paraplegia Panel

CYP4F22

Congenital Ichthyosis XomeDxSlice

CYP4F22 Gene Sequencing

CYP7B1

Comprehensive Hereditary Spastic Paraplegia Panel

Uncomplicated Hereditary Spastic Paraplegia Panel