FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term dermatopathia pigmentosa reticularis ID (Ontology) DOID:0111342 (Human Disease)
Definition An ectodermal dysplasia characterized by reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy that has_material_basis_in heterozygous mutation in the KRT14 gene on chromosome 17q21.2.
Also Known As "DPR"
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autosomal genetic disease
 |__autosomal dominant disease__
syndrome                        |
 |__ectodermal dysplasia________|
                                dermatopathia pigmentosa reticularis
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Is a autosomal dominant disease
ectodermal dysplasia
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Synonyms
  • "DPR" EXACT OMO:0003012
Secondary IDs
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GARD:8550
MESH:C535374
MIM:125595
ORDO:86920
SNOMEDCT_US_2023_03_01:239088003
UMLS_CUI:C0406778