About   Help   FAQ
Disease Ontology Browser
hereditary lymphedema II (DOID:0070213)
Alliance: disease page
Synonyms: late-onset lymphedema; LMPH2; lymphedema preacox; Meige disease; Meige lymphedema
Alt IDs: OMIM:153200, ICD10CM:I89.0, MESH:C562467, ORDO:90186, UMLS_CUI:C0238261, UMLS_CUI:C1704424
Definition: A hereditary lymphedema characterized by onset around puberty of chronic lymphedema particularly in the lower limbs with an apparent autosomal dominant pattern of inheritance.

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 		The Jackson Laboratory