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Diseases
Genes (319)
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GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
GALE
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
ACVR2B
Heterotaxy, Visceral, 7, Autosomal
SLC2A10
Arterial Tortuosity Syndrome
PQBP1
Renpenning's Syndrome
GALK1
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
MMP21
Heterotaxy, Visceral, 7, Autosomal
IFIH1
Singleton Merten Syndrome
ZIC3
Heterotaxy, Visceral, 7, Autosomal
LEFTY2
Heterotaxy, Visceral, 7, Autosomal
ALAD
Lead Poisoning
CTNS
Cystinosis
NODAL
Heterotaxy, Visceral, 7, Autosomal
GDF1
Heterotaxy, Visceral, 7, Autosomal
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CRELD1
Heterotaxy, Visceral, 7, Autosomal
TDGF1
Heterotaxy, Visceral, 7, Autosomal