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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)
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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory