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Disease Ontology Browser
hereditary lymphedema I (DOID:0070212)
Alliance: disease page
Synonyms: congenital primary lymphedema; hereditary lymphedema type I; LMPH1; Milroy disease; Nonne-Milroy lymphedema; PCL
Alt IDs: ICD10CM:Q82.0, MESH:D008209, NCI:C48829, ORDO:79452, UMLS_CUI:C1704423
Definition: A hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood.

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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory