Porokeratosis - CISMeF

Preferred Label : Porokeratosis;

NCIt definition : A clonal proliferation of abnormal keratinocytes characterized by the development of localized or multiple atrophic skin patches surrounded by an annular keratotic ring called cornoid lamella.;

Details

Origin ID

C85019;

UMLS CUI

C0162839;

Automatic exact mappings (from CISMeF team)
- Other specified congenital malformations of skin [ICD-10 Sub-category (who)]
- Porokeratoses [ICD-11 Category]
- Porokeratosis [OMIM phenotypic series]
- Porokeratosis of Mibelli (disorder) [SNOMED CT concept]
- porokeratosis of mibelli [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital pigmentary anomalies of skin [ICD-9 code]
- Porokeratosis [PASCAL descriptor]
- Porokeratosis [HPO term]
- Porokeratosis [MedDRA Preferred Term]
- Porokeratosis [ORDO Disease]
- Porokeratosis (disorder) [SNOMED CT concept]
- porokeratosis [Disease (Nov.)]
- porokeratosis [DO Concept]
- porokeratosis [MeSH Descriptor]
- porokeratosis [MeSH concept]
DO Cross reference
- porokeratosis [DO Concept]
Has associated anatomic sites
- Integumentary System [NCIt concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Porokeratosis [ORDO Disease]
- Porokeratosis [HPO term]
- Porokeratosis [MedDRA Preferred Term]
- Porokeratosis (disorder) [SNOMED CT concept]
- porokeratosis [MeSH concept]
- porokeratosis [MeSH Descriptor]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_has_finding
- Cutaneous Involvement [NCIt concept]
disease_has_primary_anatomic_site
- Skin [NCIt concept]

Keyword's position in hierarchy(ies) :

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