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Disease Ontology Browser
ectodermal dysplasia 11B (DOID:0111654)
Alliance: disease page
Synonyms: ECTD11B; ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive
Alt IDs: OMIM:614941
Definition: A hypohidrotic ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in the EDARADD gene on chromosome 1q42-q43.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/12/2024
MGI 6.24 		The Jackson Laboratory