Genetic Conditions tested at Virtus Diagnostics

HEMOCHROMATOSIS, JUVENILE, TYPE 2A

HEMOCHROMATOSIS, JUVENILE, TYPE 2B

HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2

HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3

HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4

HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5

HEMOPHILIA A

HEMOPHILIA B

HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY

HERMANSKY-PUDLAK SYNDROME 2

HERMANSKY-PUDLAK SYNDROME 9

HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 1

HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 2

HETEROTAXY, VISCERAL, 1, X-LINKED

HOLOCARBOXYLASE SYNTHETASE DEFICIENCY

HOMOCYSTINURIA

HOYERAAL-HREIDARSSON SYNDROME

HURLER SYNDROME

HYALINOSIS, INFANTILE SYSTEMIC

HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS

HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA

HYDROXYACYL-CoA DEHYDROGENASE/3-KETOACYL-CoA THIOLASE/ENOYL-CoA HYDRATASE DEFICIENCY

HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE

HYPEREKPLEXIA AND EPILEPSY

HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1

HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME

HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS

HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS, CMT3

HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS, CMT3

HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS, CMT3,

HYPOGONADOTROPIC HYPOGONADISM

HYPOMAGNESEMIA, RENAL, WITH OCULAR INVOLVEMENT

HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME

HYPOPHOSPHATASIA, CHILDHOOD

HYPOPHOSPHATEMIC OSTOPENIA, AUTOSOMAL RECESSIVE

HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4