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Diseases
Genes (848)
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ASL
Liver Failure
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
F12
Factor Xii Deficiency
SLC12A6
Andermann Syndrome
SLC17A5
Liver Failure
Acute Liver Failure
Salla Disease
PQBP1
Renpenning's Syndrome
ASS1
Liver Failure
Argininosuccinic Aciduria
Citrullinemia Type I
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
ACVR2B
Heterotaxy, Visceral, 7, Autosomal
TNF
Liver Failure
Acute Liver Failure
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Salla Disease
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
TRNL1
Liver Failure
Merrf Syndrome
IFIH1
Singleton Merten Syndrome
MMP21
Heterotaxy, Visceral, 7, Autosomal
ACTG2
Berdon Syndrome
ATP7B
Liver Failure
Acute Liver Failure
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome