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Diseases
Genes (953)
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SALL4
Duane-Radial Ray Syndrome
GJA1
Oculodentodigital Dysplasia
COL6A1
Bethlem Myopathy
FMR1
Disinhibition
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
ACADVL
Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
MMUT
Methylmalonyl-Coa Mutase Deficiency
SLC17A5
Acute Liver Failure
Liver Failure
Salla Disease
TNF
Callosity
Acute Liver Failure
Liver Failure
Salla Disease
Diverticulum
Baller–gerold Syndrome
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
ALB
Acute Liver Failure
Liver Failure
Aseptic Meningitis
Disinhibition
COL6A3
Bethlem Myopathy
COL6A2
Bethlem Myopathy
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
RECQL4
Baller–gerold Syndrome
IL6
Callosity
Acute Liver Failure
Liver Failure
Aseptic Meningitis
Familial Isolated Vitamin E Deficiency
PDGFRB
Primary Familial Brain Calcification
ASS1
Liver Failure
Citrullinemia Type I
FAM20A
Enamel-Renal Syndrome