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Diseases
Genes (761)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
IFIH1
Dry Skin
Singleton Merten Syndrome
PQBP1
Renpenning's Syndrome
ACVR2B
Heterotaxy, Visceral, 7, Autosomal
CYB5R3
Methemoglobinemia
MMP21
Heterotaxy, Visceral, 7, Autosomal
ZIC3
Heterotaxy, Visceral, 7, Autosomal
LEFTY2
Heterotaxy, Visceral, 7, Autosomal
IFNG
Legionnaires' Disease
Dry Eyes
Cryptosporidiosis
Amoebiasis
Dry Eye Syndrome
HLA-DRB1
Typhoid Fever
Dry Eyes
Amoebiasis
Dry Eye Syndrome
NODAL
Heterotaxy, Visceral, 7, Autosomal
GDF1
Heterotaxy, Visceral, 7, Autosomal
RB1
Pinealoblastoma
Trilateral Retinoblastoma
TLR5
Legionnaires' Disease
Typhoid Fever
TNFRSF1B
Legionnaires' Disease
Dry Skin
CRELD1
Heterotaxy, Visceral, 7, Autosomal
DDX58
Singleton Merten Syndrome
GSTM1
Raynaud's Disease