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DO Term : ectodermal dysplasia 14 [DOID:0111662] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An ectodermal dysplasia characterized by scalp hypotrichosis and hypodontia that has_material_basis_in homozygous or compound heterozygous mutation in the TSPEAR gene on chromosome 21q22.3.
  • synonyms:
  • ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis,
  • OMIM:618180,
  • 618180,
  • ECTN14
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents