Source:http://linkedlifedata.com/resource/umls/id/C0162359
MSH: An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.,NCI: A rare genetic disorder characterized by mutations in the gene encoding ectodysplasin A. It results in abnormalities in the morphogenesis of the structures originating from the ectoderm.