About   Help   FAQ
Disease Ontology Browser
Meesmann corneal dystrophy (DOID:0060451)
Alliance: disease page
Synonyms: juvenile hereditary epithelial dystrophy; MECD; Stocker-Holt dystrophy
Alt IDs: OMIM:122100, ICD10CM:H18.52, ICD9CM:371.51, MESH:D053559, NCI:C84795, ORDO:98954, UMLS_CUI:C0339277

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.12
The Jackson Laboratory