macular 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

macular corneal dystrophy (DOID:2565)
Alliance: disease page
Synonyms: Fehr corneal dystrophy; MACULAR DYSTROPHY, CORNEAL, 1
Alt IDs: OMIM:217800, ICD10CM:H18.55, ICD9CM:371.55, MESH:D003317, NCI:C34793, UMLS_CUI:C0024439
Definition: A corneal dystrophy that is characterized by corneal haze, bilateral loss of vision, eventually necessitating corneal transplantation resulting from progressive punctate opacities in the cornea.

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 12/10/2024 MGI 6.24