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Diseases
Genes (187)
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PRNP
Kuru, Susceptibility To
Variant Creutzfeldt–jakob Disease
TTPA
Familial Isolated Vitamin E Deficiency
SLC4A1
Southeast Asian Ovalocytosis
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
IFIH1
Singleton Merten Syndrome
SRD5A2
5α-Reductase Deficiency
PDGFB
Primary Familial Brain Calcification
RB1
Pinealoblastoma
Trilateral Retinoblastoma
DDX58
Singleton Merten Syndrome
SLC11A1
Buruli Ulcer
XPR1
Primary Familial Brain Calcification
MYORG
Primary Familial Brain Calcification
FH
Fumarase Deficiency
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
ALDH1A1
Variant Creutzfeldt–jakob Disease
H4C4
Variant Creutzfeldt–jakob Disease