Comedones, familial dyskeratotic

Preferred Label : Comedones, familial dyskeratotic;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %120450;

Details

Origin ID

120450;

UMLS CUI

C0345424;

Automatic exact mappings (from CISMeF team)
- Familial dyskeratotic comedones [PASCAL descriptor]
Currated CISMeF NLP mapping
- Familial dyskeratotic comedones (disorder) [SNOMED CT concept]
- comedones, familial dyskeratotic [MeSH concept]
- comedones, familial dyskeratotic [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the skin [HPO term]
- Autosomal dominant inheritance [HPO term]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Familial dyskeratotic comedones (disorder) [SNOMED CT concept]
- comedones, familial dyskeratotic [MeSH Supplementary Concept]
- comedones, familial dyskeratotic [MeSH concept]

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