Congenital cataract microcornea with corneal opacity

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL CATARACT MICROCORNEA WITH CORNEAL OPACITY
289499C5779991
ATOH7 Unknown
22068589
Disgenet, Orphanet —
PXDN Unknown
21907015 24939590
Disgenet, Orphanet
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Congenital cataract microcornea with corneal opacity.
5 View disease cluster →
anterior segment dysgenesis 7 1 shared genePXDN Related via 1 shared gene including PXDN. Anterior segment dysgenesis 2 shared genesATOH7, PXDN Related via 2 shared genes including ATOH7, PXDN. Anterior segment mesenchymal dysgenesis 1 shared genePXDN Related via 1 shared gene including PXDN. Visual disorder 1 shared genePXDN Related via 1 shared gene including PXDN. Systemic sclerosis 1 shared genePXDN Related via 1 shared gene including PXDN.