Setting-sun phenomenon, familial benign

Preferred Label : Setting-sun phenomenon, familial benign;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Multifactorial vs. autosomal dominant;

Prefixed ID : 600598;

Details

Origin ID

600598;

UMLS CUI

C1833577;

Currated CISMeF NLP mapping
- Setting-Sun phenomenon, familial benign [MeSH concept]
- Setting-Sun phenomenon, familial benign [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the eye [HPO term]
- Autosomal dominant inheritance [HPO term]
- Multifactorial inheritance [HPO term]
- Upper eyelid retraction [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Setting-Sun phenomenon, familial benign [MeSH Supplementary Concept]
- Setting-Sun phenomenon, familial benign [MeSH concept]

Keyword's position in hierarchy(ies) :

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