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Diseases
Genes (797)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
IFIH1
Japanese Encephalitis
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
Traveler's Diarrhea
PDGFB
Callosity
Primary Familial Brain Calcification
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma
TNF
Japanese Encephalitis
Callosity
Cholera
Pleural Effusion
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
FUT2
Norovirus Infection
ITGB3
Japanese Encephalitis
Coronary Thrombosis
DDX58
Japanese Encephalitis
Singleton Merten Syndrome
XPR1
Primary Familial Brain Calcification
MYORG
Primary Familial Brain Calcification
PLAT
Coronary Thrombosis
LMOD1
Berdon Syndrome
APOB
Cholera
Familial Isolated Vitamin E Deficiency
PTPN22
Giant Cell Arteritis