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Diseases
Genes (332)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
IFIH1
Singleton Merten Syndrome
DMPK
Myotonic Dystrophy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CNBP
Myotonic Dystrophy
IFNG
Filariasis
Ascariasis
Trichuriasis
DDX58
Singleton Merten Syndrome
CYP2A6
Opisthorchiasis
Myotonic Dystrophy
NKX2-5
Myotonic Dystrophy
MPO
Trichuriasis
APOB
Familial Isolated Vitamin E Deficiency
APOA1
Familial Isolated Vitamin E Deficiency
IL4
Nematode Infection
Filariasis
CYP1A1
Nematode Infection
MUC4
Nematode Infection
TNFRSF1A
Nematode Infection
MUC2
Nematode Infection
FAS
Clonorchiasis
FASLG
Clonorchiasis