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Echinobase
Summary Literature (0)
DOID:0070210 - hereditary lymphedema IA

Disease Ontology Definition:A hereditary lymphedema characterized by autosomal dominant inheritance that has_material_basis_in mutation in the FLT4 gene on chromosome 5q35.

Synonyms: LMPH1A

Echinobase Genes : flt4


MIM:
MIM:153100 - lymphedema, hereditary, ia; lmph1a

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)