OBO ID: DOID:0111342 |
Term Name: | dermatopathia pigmentosa reticularis | Search Ontology: | |
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Synonyms: |
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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. (2) | ||
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Ontology: | Human Disease ( DOID:0111342 ) |
OTHER dermatopathia pigmentosa reticularis PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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KRT14 | Dermatopathia pigmentosa reticularis |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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