Vocal cord paralysis and ptosis

Preferred Label : Vocal cord paralysis and ptosis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 193240;

Details

Origin ID

193240;

UMLS CUI

C1860403;

Currated CISMeF NLP mapping
- Ptosis and vocal cord paralysis syndrome (disorder) [SNOMED CT concept]
- Ptosis-vocal cord paralysis syndrome [ORDO Disease]
- Tucker syndrome [MeSH concept]
- tucker syndrome [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Bilateral ptosis [HPO term]
- Vocal cord paralysis [HPO term]
ORDO concept(s)
- Ptosis-vocal cord paralysis syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ptosis and vocal cord paralysis syndrome (disorder) [SNOMED CT concept]
- Ptosis-vocal cord paralysis syndrome [ORDO Disease]
- Tucker syndrome [MeSH concept]
- tucker syndrome [MeSH Supplementary Concept]

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