persistent hyperplastic primary vitreous Disease Ontology Browser

Home
Genes
Phenotypes
Human Disease
Expression
Recombinases
Function
Strains / SNPs
Homology
Tumors

About Help FAQ

Search
Download
More Resources
Submit Data
Find Mice (IMSR)
Analysis Tools
Contact Us
Browsers

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)
Citing These Resources Funding Information Warranty Disclaimer, Copyright, and Privacy Statement Send questions and comments to User Support.	last database update 01/31/2023 MGI 6.22

Allelic Composition	Genetic Background	Reference	Phenotypes
Tg(NES/TK-PDGFB,-lacZ)310Kfn/0	B6.Cg-Tg(NES/TK-PDGFB,-lacZ)310Kfn	J:189829	View