Meesmann corneal dystrophy 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

Meesmann corneal dystrophy (DOID:0060451)
Alliance: disease page
Synonyms: juvenile hereditary epithelial dystrophy; MECD; Stocker-Holt dystrophy
Alt IDs: ICD10CM:H18.52, ICD9CM:371.51, MESH:D053559, NCI:C84795, OMIM:PS122100, ORDO:98954, UMLS_CUI:C0339277
Definition: An epithelial and subepithelial dystrophy that is characterized by the formation of tiny round cysts in the corneal epithelium.

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, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Krt12tm1.1(KRT12L132P)Arte/Krt12tm1.1(KRT12L132P)Arte	involves: C57BL/6	J:229462	View