Genetic Conditions tested at Virtus Diagnostics

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Disease
Code
Fur Further Information
ODONTOONYCHODERMAL DYSPLASIA
WNT10A
OF FINGERS & TOES
GJB2
OMENN SYNDROME
DCLRE1C
OPITZ GBBB SYNDROME, X-LINKED
MID1
OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA
TIMM8A
ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO
OTC
OSTEOGENESIS IMPERFECTA, TYPE IIB
CRTAP
OSTEOGENESIS IMPERFECTA, TYPE VIII
LEPRE1
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1
TCIRG1
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3
CA2
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 4
CLCN7
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5
OSTM1