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Diseases
Genes (941)
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ASL
Liver Failure
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
SALL4
Duane-Radial Ray Syndrome
SLC6A19
Hartnup Disease
GJA1
Oculodentodigital Dysplasia
COL6A1
Bethlem Myopathy
FMR1
Disinhibition
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Fg Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
ACADVL
Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
MMUT
Methylmalonyl-Coa Mutase Deficiency
SLC17A5
Acute Liver Failure
Liver Failure
Salla Disease
TNF
Acute Liver Failure
Liver Failure
Salla Disease
Baller–gerold Syndrome
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Uremia
ALB
Acute Liver Failure
Liver Failure
Aseptic Meningitis
Disinhibition
Uremia
COL6A3
Bethlem Myopathy
COL6A2
Bethlem Myopathy
PQBP1
Renpenning's Syndrome
ASS1
Liver Failure
Argininosuccinic Aciduria
Citrullinemia Type I
RECQL4
Baller–gerold Syndrome
IL6
Acute Liver Failure
Liver Failure
Argininosuccinic Aciduria
Aseptic Meningitis
Familial Isolated Vitamin E Deficiency
Uremia
MED12
Fg Syndrome