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Summary Literature (0)
DOID:0111649 - ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome


Disease Ontology Definition:An ectodermal dysplasia characterized by ectodermal dysplasia, ectrodactyly, and macular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the CDH3 gene on chromosome 16q22.1.

Synonyms: ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome, EEMS, EEM syndrome

Xenbase Genes : cdh3



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), ectodermal dysplasia (is_a)