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Diseases
Genes (650)
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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
Japanese Encephalitis
Singleton Merten Syndrome
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
Japanese Encephalitis
Pleural Effusion
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Bloom Syndrome
ITGB3
Japanese Encephalitis
Coronary Thrombosis
Bloom Syndrome
DDX58
Japanese Encephalitis
Singleton Merten Syndrome
UNG
Bloom Syndrome
PLAT
Coronary Thrombosis
Bloom Syndrome
XPR1
Primary Familial Brain Calcification