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Diseases
Genes (808)
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ASL
Liver Failure
Argininosuccinic Aciduria
EFHC1
Juvenile Myoclonic Epilepsy
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Juvenile Myoclonic Epilepsy
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
TNF
Liver Failure
Acute Liver Failure
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Salla Disease
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
GABRA1
Juvenile Myoclonic Epilepsy
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
ATP7B
Liver Failure
Acute Liver Failure
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CACNB4
Juvenile Myoclonic Epilepsy
JRK
Juvenile Myoclonic Epilepsy