hereditary choroidal atrophy

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Summary

Literature (0)

DOID:9794 - hereditary choroidal atrophy

Disease Ontology Definition:n_a

Synonyms:

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

: prph2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0004883 - lung mesenchyme

MONDO:0004883 - lung mesenchyme

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

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

Parent(s): choroidal sclerosis (is_a)