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Summary Literature (0)
DOID:0060838 - isolated microphthalmia 7

Disease Ontology Definition:An isolated microphthalmia characterized by unilateral microphthalmia that has_material_basis_in caused by mutation in the GDF3 gene on chromosome 12p13.

Synonyms: MCOP7

Xenbase Genes : gdf3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013377 - isolated microphthalmia 7

MIM:
MIM:613704 - MICROPHTHALMIA, ISOLATED 7; MCOP7

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autosomal dominant disease (is_a), isolated microphthalmia (is_a), microphthalmia (is_a)