Genetic Conditions tested at Virtus Diagnostics

CANAVAN DISEASE

CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO

CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE

CARDIOMYOPATHY, DILATED, 3A

CARNITINE DEFICIENCY, SYSTEMIC PRIMARY

CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL

CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY

CARPENTER SYNDROME

CARTILAGE-HAIR HYPOPLASIA

CEREBELLAR HYPOPLASIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDAL LOCOMOTION

CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMA

CEREBROOCULOFACIOSKELETAL SYNDROME 1

CEREBROTENDINOUS XANTHOMATOSIS

CEROID LIPOFUSCINOSIS, NEURONAL, 10

CEROID LIPOFUSCINOSIS, NEURONAL, 3

CEROID LIPOFUSCINOSIS, NEURONAL, 5

CEROID LIPOFUSCINOSIS, NEURONAL, 6

CEROID LIPOFUSCINOSIS, NEURONAL, 7

CEROID LIPOFUSCINOSIS, NEURONAL, 8

CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT

CHARCOT-MARIE-TOOTH DISEASE TYPE 4A

CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H

CHEDIAK HIGASHI SYNDROME

CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1

CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2

CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 3

CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE

CHONDRODYSPLASIA, BLOMSTRAND TYPE

CITRULLINEMIA, CLASSIC

COCKAYNE SYNDROME TYPE B

COCKAYNE SYNDROME, TYPE A

COENZYME Q10 DEFICIENCY

COENZYME Q10 DEFICIENCY

COENZYME Q10 DEFICIENCY

COENZYME Q10 DEFICIENCY

COENZYME Q10 DEFICIENCY

COENZYME Q10 DEFICIENCY

COFFIN-LOWRY SYNDROME CLS

COHEN SYNDROME

COMBINED IMMUNODEFICIENCY, X-LINKED

COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1

COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2

COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3

COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4

COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5

COMBINED SAPOSIN DEFICIENCY

Complex I Deficiency

Complex I Deficiency

Complex I Deficiency

Complex I Deficiency

Complex I Deficiency

Complex I Deficiency

Complex I Deficiency

Complex I Deficiency

Complex I Deficiency

Complex I Deficiency

Complex I Deficiency

Complex IV deficiency

Complex IV deficiency

Complex IV deficiency

Complex IV deficiency

Complex IV deficiency

Complex IV deficiency

CONGENITAL ADRENAL HYPERPLASIA

CONGENITAL ADRENAL HYPERPLASIA

CONGENITAL ADRENAL HYPERPLASIA, LIPOID

CONGENITAL ADRENAL HYPOPLASIA

CONGENITAL DEAFNESS WITH KERATOPACHYDERMIA & CONSTRICTIONS OF FINGERS AND TOES

CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1A

CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1C

CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1G

CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1I

CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1M

CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2d

CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2G

CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2H

CONGENITAL DISORDER OF GLYCOSYLATION TYPE2B

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1B

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1D

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1E

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1F

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1H

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1J

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1K

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1L

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1N

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1Q

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 2C

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 2E

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 2F

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE2A

CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS

CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA

CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED

CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY

CRANIOFRONTONASAL SYNDROME

CREATINE DEFICIENCY SYNDROME, X-LINKED

CRISPONI SYNDROME

CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE 1A

CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE 2

CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE I

CYSTIC FIBROSIS

CYSTINOSIS, ADULT NONNEPHROPATHIC

CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE

CYSTINOSIS, NEPHROPATHIC