congenital symblepharon Disease Ontology Browser

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Disease Ontology Browser

congenital symblepharon (DOID:0111720)
Alliance: disease page
Alt IDs: ORDO:98948
Definition: An isolated cryptophthalmia characterized by fusion of the upper eyelid skin to the superior aspect of the globe often associated with microphthalmia.

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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