hereditary lymphedema II

Summary

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: late-onset lymphedema, LMPH2, lymphedema preacox, Meige disease, Meige lymphedema

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: foxc2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007920 - lymphatic malformation 5

MONDO:0007920 - lymphatic malformation 5

MIM:

MIM:153200 - LYMPHATIC MALFORMATION 5; LMPHM5

MIM:153200 - LYMPHATIC MALFORMATION 5; LMPHM5

Other Model Organisms: Alliance, 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)