Cheilitis glandularis

Preferred Label : Cheilitis glandularis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 118330;

Details

Origin ID

118330;

UMLS CUI

C0267034;

Automatic exact mappings (from CISMeF team)
- Diseases of lips [ICD-10 Sub-category (who)]
- Glandular cheilitis [ICD-11 More detail]
- cheilitis [MeSH Descriptor]
Currated CISMeF NLP mapping
- Cheilitis glandularis [MeSH concept]
- Cheilitis glandularis [ORDO Disease]
- Cheilitis glandularis (disorder) [SNOMED CT concept]
- cheilitis glandularis [MeSH Supplementary Concept]
- cheilitis glandularis, nos [SNOMED Notion]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Carcinoma [HPO term]
- Cheilitis [HPO term]
- Enlarged everted lower lip [HPO term]
- Everted lower lip vermilion [HPO term]
- Squamous cell carcinoma [HPO term]
- Vascular dilatation [HPO term]
ORDO concept(s)
- Cheilitis glandularis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cheilitis glandularis [ORDO Disease]
- Cheilitis glandularis [MeSH concept]
- Cheilitis glandularis (disorder) [SNOMED CT concept]
- cheilitis glandularis [MeSH Supplementary Concept]
- cheilitis glandularis, nos [SNOMED Notion]
- simple cheilitis glandularis [SNOMED Notion]

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