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Disease Ontology Browser
ectodermal dysplasia 15 (DOID:0111651)
Alliance: disease page
Synonyms: ECTD15; ectodermal dysplasia 15, hypohidrotic/hair type
Alt IDs: OMIM:618535
Definition: An ectodermal dysplasia characterized by onset in early childhood of hypotrichosis and absence of sweating except with extreme exercise that has_material_basis_in homozygous or compound heterozygous mutation in the CST6 gene on chromosome 11q13.1.

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