ectodermal dysplasia 11B

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Summary

Literature (0)

DOID:0111654 - ectodermal dysplasia 11B

Disease Ontology Definition:A hypohidrotic ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in the EDARADD gene on chromosome 1q42-q43.

Synonyms: ECTD11B, ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive,

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

: edaradd

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), hypohidrotic ectodermal dysplasia (is_a)