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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:
OMIM:269400 - ANTERIOR SEGMENT DYSGENESIS 7; ASGD7 |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

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