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Diseases
Genes (329)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC4A1
Southeast Asian Ovalocytosis
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
IFIH1
Singleton Merten Syndrome
SRD5A2
5α-Reductase Deficiency
PRNP
Kuru, Susceptibility To
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
PRSS56
Cystic Eyeball
DICER1
Pinealoblastoma
PCYT1B
Cholera
CTBS
Cholera