ectodermal dysplasia 10B

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

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

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 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

: edar, edaradd

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

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

Xenbase: The Xenopus Model Organism Knowledgebase.
Version: 4.14.0

Major funding for Xenbase is provided by grant P41 HD064556