centronuclear myopathy X-linked 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

centronuclear myopathy X-linked (DOID:0111225)
Alliance: disease page
Synonyms: CNMX; MTM1; myotubular myopathy 1; X-linked myotubular myopathy; XLCNM; XLMTM
Alt IDs: OMIM:310400, ICD10CM:G71.220, MESH:D020914, NCI:C118781, ORDO:596, UMLS_CUI:C0410203
Definition: A centronuclear myopathy that has_material_basis_in X-linked inheritance of mutations in MTM1 on Xq28.

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 11/12/2024 MGI 6.24