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Summary Literature (0)
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,

Xenbase Genes : foxc2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007920 - lymphatic malformation 5

OMIM:
OMIM:153200 - LYMPHATIC MALFORMATION 5; LMPHM5

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), hereditary lymphedema (is_a)