congenital aphakia

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Summary

Literature (0)

DOID:11367 - congenital aphakia

Disease Ontology Definition:n_a

Synonyms: APHAKIA, CONGENITAL PRIMARY, Congenital absence of lens

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: foxe3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012456 - congenital primary aphakia

MONDO:0012456 - congenital primary aphakia

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): lens disease (is_a), physical disorder (is_a)