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Disease Ontology Browser
persistent hyperplastic primary vitreous (DOID:0060282)
Alliance: disease page
Alt IDs: OMIM:221900, OMIM:611308, MESH:D054514, NCI:C161554, ORDO:91495, UMLS_CUI:C0266568
Definition: A developmental vitreous disease that is characterized by leukocoria, strabismus and vision loss, caused by failure of primary vitreous and hyaloid vasculature to regress during embryological development.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/31/2023
MGI 6.22
The Jackson Laboratory