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DO Term : ectodermal dysplasia 15 [DOID:0111651] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • 618535,
  • ECTD15,
  • ectodermal dysplasia 15, hypohidrotic/hair type,
  • OMIM:618535
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents