Virtus Genetics
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Genes & Diseases - What we test for

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Disease
Code
Fur Further Information
ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH IMMUNE DEFICIENCY
IKBKG
ECTODERMAL DYSPLASIA, HYPOHIDROTIC, X-LINKED
EDA
ELEJALDE DISEASE
MYO5A
ELLIS-VAN CREVELD SYNDROME
EVC
ENCEPHALOPATHY, ETHYLMALONIC
ETHE1
EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE
COL7A1
EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA
ITGA6
EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY
PLEC1
EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE
LAMA3
EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE
COL17A1
EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC
DSP
EPILEPSY, FEMALE-RESTRICTED, WITH MENTAL RETARDATION
PCDH19
EPILEPSY, PYRIDOXINE-DEPENDENT
ALDH7A1
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1
ARX
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3
SLC25A22
EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS
EIF2AK3
menuchevron-down