FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term ectodermal dysplasia 15 ID (Ontology) DOID:0111651 (Human Disease)
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.
Also Known As "ECTD15" ; "ectodermal dysplasia 15, hypohidrotic/hair type"
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 Genes
 ectodermal dysplasia 15       3
 for disease ribbon | ectodermal dysplasia 15       3
 model of | ectodermal dysplasia 15       3
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
syndrome                         |
 |__ectodermal dysplasia_________|
                                 ectodermal dysplasia 15  3 rec.
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Is a autosomal recessive disease
ectodermal dysplasia
Part of
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Synonyms
  • "ECTD15" EXACT OMO:0003012
    "ectodermal dysplasia 15, hypohidrotic/hair type" EXACT
Secondary IDs
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MIM:618535