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DOID:0060451 - Meesmann corneal dystrophy
Disease Ontology Definition:n_a
Synonyms: MECD, Stocker-Holt dystrophy, juvenile hereditary epithelial dystrophy,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:122100 - corneal dystrophy, meesmann; mecd |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee