Brittle cornea syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
BRITTLE CORNEA SYNDROME 1
229200MESH:C536192MONDO:0024543
ZNF469 Causal
18452888 19661234 20938016
CTD, ClinVar, GWAS catalog, HPO —
BRITTLE CORNEA SYNDROME 2
614170C3280011MONDO:0013605OMIM:614170
PRDM5 Causal
21664999 27032025 22122778
CTD, ClinVar, Disgenet, GWAS catalog, HPO —
All2 Causal2 Unknown2
Related Diseases Diseases that share the most curated genes with Brittle cornea syndrome.
5 View disease cluster →
Axenfeld-rieger syndrome 1 shared genePRDM5 Related via 1 shared gene including PRDM5. Aortic disease 2 shared genesPRDM5, ZNF469 Related via 2 shared genes including PRDM5, ZNF469. Congenital skin anomaly 1 shared geneZNF469 Related via 1 shared gene including ZNF469. Skin abnormalities 1 shared geneZNF469 Related via 1 shared gene including ZNF469. Corneal disease 1 shared geneZNF469 Related via 1 shared gene including ZNF469.