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
90354MONDO:0009242
PRDM5 Unknown
21664999
ClinVar, Orphanet —
ZNF469 Unknown
19661234 20938016
HPO, Orphanet —
All2 Causal2 Unknown2
Related Diseases Diseases that share the most curated genes with Brittle cornea syndrome.
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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.