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Diseases
Genes (644)
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TTPA
Familial Isolated Vitamin E Deficiency
BLM
Bloom Syndrome
SLC20A2
Primary Familial Brain Calcification
PQBP1
Renpenning's Syndrome
PDGFRB
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
Japanese Encephalitis
ACTG2
Berdon Syndrome
PDGFB
Primary Familial Brain Calcification
MYH11
Berdon Syndrome
ASS1
Citrullinemia Type I
MYLK
Berdon Syndrome
MEN1
Glucagonoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
TNF
Pleural Effusion
Japanese Encephalitis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Bloom Syndrome
ITGB3
Coronary Thrombosis
Japanese Encephalitis
Bloom Syndrome
DDX58
Singleton Merten Syndrome
Japanese Encephalitis
UNG
Bloom Syndrome
XPR1
Primary Familial Brain Calcification
MYORG
Primary Familial Brain Calcification