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Diseases
Genes (878)
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ASL
Liver Failure
Argininosuccinic Aciduria
TNF
Liver Failure
Acute Liver Failure
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Tachycardia
Salla Disease
PMM2
Pmm2 Deficiency
SLC6A19
Hartnup Disease
TTPA
Familial Isolated Vitamin E Deficiency
F12
Factor Xii Deficiency
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
SLC17A5
Liver Failure
Acute Liver Failure
Salla Disease
ASS1
Liver Failure
Argininosuccinic Aciduria
Citrullinemia Type I
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UMOD
Medullary Cystic Kidney Disease
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
TRNL1
Liver Failure
Merrf Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
ATP7B
Liver Failure
Acute Liver Failure
INS
Acute Liver Failure
Tachycardia