FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term ectodermal dysplasia 14 ID (Ontology) DOID:0111662 (Human Disease)
Definition 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.
Also Known As "ECTN14" ; "ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis" ; "hypohidrotic/hair/tooth/nail type"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 ectodermal dysplasia 14       1
 for disease ribbon | ectodermal dysplasia 14       1
 model of | ectodermal dysplasia 14       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal recessive disease__
syndrome                         |
 |__ectodermal dysplasia_________|
                                 ectodermal dysplasia 14  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal recessive disease
ectodermal dysplasia
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "ECTN14" EXACT OMO:0003012
    "ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis" EXACT
    "hypohidrotic/hair/tooth/nail type" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MIM:618180