Genetic Conditions tested at Virtus Diagnostics

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Disease
Code
Fur Further Information
BARTH SYNDROME
TAZ
BARTTER SYNDROME, ANTENATAL, TYPE 1
SLC12A1
BARTTER SYNDROME, ANTENATAL, TYPE 2
KCNJ1
BETA-HYDROXYISOBUTYRYL CoA DEACYLASE, DEFICIENCY OF
HIBCH
BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4
AMACR
BIOTINIDASE DEFICIENCY
BTD
BLOOM SYNDROME
BLM
BRANCHED-CHAIN KETO ACID DEHYDROGENASE E1, BETA POLYPEPTIDE
BCKDHB
BRITTLE CORNEA SYNDROME (Ehlers-Danlos syndrome type VIB)
ZNF469