Ptosis, strabismus, and ectopic pupils

Preferred Label : Ptosis, strabismus, and ectopic pupils;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 178330;

Details

Origin ID

178330;

UMLS CUI

C1867437;

Currated CISMeF NLP mapping
- Ptosis-strabismus-ectopic pupils syndrome [ORDO Disease]
- ptosis, strabismus, and ectopic pupils [MeSH concept]
- ptosis, strabismus, and ectopic pupils [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Ptosis [HPO term]
- Strabismus [HPO term]
ORDO concept(s)
- Ptosis-strabismus-ectopic pupils syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ptosis-strabismus-ectopic pupils syndrome [ORDO Disease]
- ptosis, strabismus, and ectopic pupils [MeSH Supplementary Concept]
- ptosis, strabismus, and ectopic pupils [MeSH concept]

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