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Diseases
Genes (1060)
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SLC6A19
Hartnup Disease
TTPA
Familial Isolated Vitamin E Deficiency
FECH
Liver Failure
Erythropoietic Protoporphyria
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
SLC17A5
Liver Failure
Acute Liver Failure
Salla Disease
TNF
Liver Failure
Acute Liver Failure
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Adenoid Cystic Carcinoma
Salla Disease
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
ASS1
Liver Failure
Citrullinemia Type I
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
ATP7B
Liver Failure
Acute Liver Failure
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CD55
Protein Losing Enteropathy
ATM
Acute Liver Failure
Adenoid Cystic Carcinoma
TP53
Liver Failure
Acute Liver Failure
Adenoid Cystic Carcinoma
MPV17
Liver Failure
Acute Liver Failure