ectodermal dysplasia 11B

Summary

DOID:0111654 - ectodermal dysplasia 11B

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

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

In OMIM:

OMIM:614941 - ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B

OMIM:614941 - ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B

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

: edaradd

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

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