Genetic Conditions tested at Virtus Diagnostics

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Disease
Code
Fur Further Information
HEMOCHROMATOSIS, JUVENILE, TYPE 2A
HJV
HEMOCHROMATOSIS, JUVENILE, TYPE 2B
HAMP
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2
PRF1
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3
UNC13D
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4
STX11
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5
STXBP2
HEMOPHILIA A; HEMA
F8
HEMOPHILIA B; HEMB
F9
HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY VODI
SP110
Hermansky Pudlak Syndrome, 9
PLDN
HERMANSKY-PUDLAK SYNDROME 2
AP3B1
HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 1
UNC93B1
HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 2
TLR3
HETEROTAXY, VISCERAL, 1, X-LINKED
ZIC3
HOLOCARBOXYLASE SYNTHETASE DEFICIENCY
HLCS
HOMOCYSTINURIA
CBS
HONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE
ARSE
HOYERAAL-HREIDARSSON SYNDROME
DKC1
HURLER SYNDROME
IDUA
HYALINOSIS, INFANTILE SYSTEMIC
ANTXR2
HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS
L1CAM
HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA
LBR
HYDROXYACYL-CoA DEHYDROGENASE/3-KETOACYL-CoA THIOLASE/ENOYL-CoA HYDRATASE DEF.
HADHA
HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE
DOCK8
HYPEREKPLEXIA AND EPILEPSY
ARHGEF9
HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1
ABCC8
HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME
SLC25A15
HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS
PMP22
HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS CMT3,
EGR2
HYPOGONADOTROPIC HYPOGONADISM
GNRHR
HYPOMAGNESEMIA, RENAL, WITH OCULAR INVOLVEMENT
CLDN19
HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME
TBCE
HYPOPHOSPHATASIA, CHILDHOOD
ALPL
HYPOPHOSPHATEMIC osteopenia, AUTOSOMAL RECESSIVE
DMP1
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4
TSHB