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DOID:0070213 - hereditary lymphedema II
Disease Ontology 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.
Synonyms: LMPH2, Meige disease, Meige lymphedema, late-onset lymphedema, lymphedema preacox
OMIM:153200 - LYMPHATIC MALFORMATION 5; LMPHM5 |
MONDO:0007920 - Meige disease |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s):
hereditary lymphedema (is_a)