Blepharochalasis and double lip

Preferred Label : Blepharochalasis and double lip;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Ascher syndrome;

Inheritance : Autosomal dominant;

Prefixed ID : 109900;

Détails

Origin ID

109900;

UMLS CUI

C0339085;

Currated CISMeF NLP mapping
- Ascher syndrome [PASCAL descriptor]
- Ascher syndrome [ICD-11 More detail]
- Ascher syndrome [ORDO Disease]
- Ascher's syndrome (disorder) [SNOMED CT concept]
- ascher's syndrome [SNOMED Notion]
- blepharochalasis and double lip [MeSH concept]
- blepharochalasis and double lip [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the eye [HPO term]
- Abnormality of the mouth [HPO term]
- Autosomal dominant inheritance [HPO term]
- Blepharochalasis [HPO term]
- Duplication of the upper lip [HPO term]
- Goiter [HPO term]
ORDO concept(s)
- Ascher syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ascher syndrome [ORDO Disease]
- Ascher's syndrome (disorder) [SNOMED CT concept]
- ascher's syndrome [SNOMED Notion]
- blepharochalasis and double lip [MeSH Supplementary Concept]
- blepharochalasis and double lip [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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