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Summary Literature (0)
DOID:0111665 - ectodermal dysplasia 10B


Disease Ontology Definition:A hypohidrotic ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in EDAR on chromosome 2q13.

Synonyms: ECTD10B, ectodermal dysplasia 10B, hypohidrotic/hair/nail type, autosomal recessive

Referenced OMIM:
OMIM:224900 - ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : edar, edaradd

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive disease (is_a), hypohidrotic ectodermal dysplasia (is_a)


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