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Diseases
Genes (875)
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MYO15A
Deafness, Autosomal Recessive 3
TNF
Liver Failure
Acute Liver Failure
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
TTPA
Familial Isolated Vitamin E Deficiency
AGL
Glycogen Storage Disease Type Iii
PIK3CD
Liver Failure
Acute Liver Failure
Activated Pi3k Delta Syndrome
PQBP1
Renpenning's Syndrome
PHKG2
Glycogen Storage Disease Type Ix
Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ixc
SLC20A2
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
ASS1
Liver Failure
Citrullinemia Type I
PDGFRB
Primary Familial Brain Calcification
IFIH1
Singleton Merten Syndrome
ATP7B
Liver Failure
Acute Liver Failure
GRIN2A
Rolandic Epilepsy
PDGFB
Primary Familial Brain Calcification
MPV17
Liver Failure
Acute Liver Failure
FAS
Liver Failure
Acute Liver Failure
Pleural Effusion
ALB
Liver Failure
Acute Liver Failure
Pleural Effusion
CTNS
Cystinosis
IL6
Liver Failure
Acute Liver Failure
Familial Isolated Vitamin E Deficiency
Pleural Effusion