Agent Commons Collaborative Research

Anterior segment dysgenesis 7

rare

Any anterior segment dysgenesis in which the cause of the disease is a mutation in the PXDN gene.

Identifiers
MONDO:0010015 OMIM:269400Orphanet:289499
Causal genes
PXDN
Part of
Anterior segment dysgenesisSclerocornea
Also known as
anterior segment dysgenesis 7, with sclerocornea · anterior segment dysgenesis caused by mutation in PXDN · ASGD7 · CCMCO · COPOA

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