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Diseases
Genes (605)
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TTPA
Familial Isolated Vitamin E Deficiency
WRN
Werner Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
ATXN3
Spinocerebellar Ataxia Type 3
IFIH1
Singleton Merten Syndrome
PDGFB
Primary Familial Brain Calcification
RB1
Pinealoblastoma
Trilateral Retinoblastoma
FUT2
Norovirus Infection
DDX58
Singleton Merten Syndrome
XPR1
Primary Familial Brain Calcification
MYORG
Primary Familial Brain Calcification
APOB
Cholera
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
Werner Syndrome
SMOC1
Klippel-Trenaunay-Weber Syndrome
SLC18A2
Spinocerebellar Ataxia Type 3
Psychotic Depression
PRSS56
Cystic Eyeball
TH
Spinocerebellar Ataxia Type 3