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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CORNEAL DYSTROPHY COL17A1 Causal — Disgenet
GRHL2 Causal — Disgenet —
SLC4A11 Causal — Disgenet —
TGFBI Causal — Disgenet
ZEB1 Causal — Disgenet
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1 COL8A2 Causal ClinVar, Disgenet, GWAS catalog, HPO
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3 TCF4 Causal — CTD, ClinVar, Disgenet, GenCC, HPO
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4 SLC4A11 Causal CTD, ClinVar, Disgenet, GWAS catalog, HPO —
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6 ZEB1 Causal — CTD, ClinVar, Disgenet, GenCC, HPO
CORNEAL DYSTROPHY, LATTICE TYPE 3A TGFBI Causal — ClinVar
CORNEAL DYSTROPHY, MEESMANN, 1 KRT12 Causal ClinVar, Disgenet, GWAS catalog, HPO
CORNEAL DYSTROPHY, MEESMANN, 2 KRT3 Causal ClinVar, Disgenet, GWAS catalog, HPO
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4 GRHL2 Causal — ClinVar, Disgenet, HPO —
CORNEAL DYSTROPHY, PUNCTIFORM AND POLYCHROMATIC PRE-DESCEMET PRDX3 Causal ClinVar, Disgenet, GWAS catalog, HPO
CORNEAL DYSTROPHY-PERCEPTIVE DEAFNESS SYNDROME SLC4A11 Causal ClinVar, GWAS catalog, Orphanet —
All32 Causal10 Unknown29