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Summary Literature (0)
DOID:0080612 - anterior segment dysgenesis 7

Disease Ontology Definition:An anterior segment dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25.

Synonyms:

In OMIM:
OMIM:269400 - ANTERIOR SEGMENT DYSGENESIS 7; ASGD7


Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : pxdn

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive disease (is_a), corneal opacification and other ocular anomalies (is_a)