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Diseases
Genes (211)
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PRNP
Kuru, Susceptibility To
Akinetic Mutism
Variant Creutzfeldt–jakob Disease
TTPA
Familial Isolated Vitamin E Deficiency
BMPR1A
Juvenile Polyposis Syndrome
SMAD4
Juvenile Polyposis Syndrome
SLC4A1
Southeast Asian Ovalocytosis
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
ENG
Juvenile Polyposis Syndrome
SRD5A2
5α-Reductase Deficiency
ASS1
Citrullinemia Type I
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PTEN
Juvenile Polyposis Syndrome
DDX58
Singleton Merten Syndrome
SLC11A1
Buruli Ulcer
FH
Fumarase Deficiency
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
ALDH1A1
Variant Creutzfeldt–jakob Disease