Genetic Conditions tested at Virtus Diagnostics

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Disease
Code
Fur Further Information
LACTIC ACIDOSIS, FATAL INFANTILE (mtDNA depletion)
SUCLG1
LARYNGOONYCHOCUTANEOUS SYNDROME
LAMA3
LATHOSTEROLOSIS
SC5DL
LEIGH SYNDROME
SURF1
LEIGH SYNDROME, FRENCH-CANADIAN TYPE
LRPPRC
LEIGH SYNDROME, X-LINKED
PDHA1
LESCH-NYHAN SYNDROME
HPRT1
LETHAL CONGENITAL CONTRACTURE SYNDROME 1
GLE1
LETHAL CONGENITAL CONTRACTURE SYNDROME 2
ERBB3
LEUKOCYTE ADHESION DEFICIENCY TYPE III
FERMT3
LEUKODYSTROPHY, HYPOMYELINATING, 2
GJC2
LEUKODYSTROPHY, HYPOMYELINATING, 5
FAM126A
LIPOID CONGENITAL ADRENAL HYPERPLASIA
CYP11A1
LISSENCEPHALY 2
RELN
LISSENCEPHALY 3
TUBA1a
LISSENCEPHALY, X-LINKED, 1
DCX
LISSENCEPHALY, X-LINKED, 2
ARX
LOWE OCULOCEREBRORENAL SYNDROME
OCRL
LUJAN-FRYNS SYNDROME
MED12
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1
SH2D1A
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2
XIAP