Laryngeal abductor paralysis, X-linked

Preferred Label : Laryngeal abductor paralysis, X-linked;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Plott syndrome; Vocal cord dysfunction, familial;

Inheritance : X-linked recessive;

Prefixed ID : 308850;

Details

Origin ID

308850;

UMLS CUI

C5886766;

Currated CISMeF NLP mapping
- Laryngeal abductor paralysis [ICD-11 More detail]
- Laryngeal abductor paralysis [ORDO Disease]
- Laryngeal abductor paralysis with intellectual disability syndrome (disorder) [SNOMED CT concept]
- Laryngeal abductor paralysis-intellectual disability syndrome [ORDO Disease]
- Vocal cord dysfunction familial [MeSH concept]
- vocal cord dysfunction familial [MeSH Supplementary Concept]
HPO term(s)
- Congenital laryngeal stridor [HPO term]
- Intellectual disability [HPO term]
- Paralysis [HPO term]
- X-linked recessive inheritance [HPO term]
ORDO concept(s)
- Laryngeal abductor paralysis-intellectual disability syndrome [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital laryngeal abductor palsy (disorder) [SNOMED CT concept]
- Laryngeal abductor paralysis [ORDO Disease]
- Laryngeal abductor paralysis-intellectual disability syndrome [ORDO Disease]
- Vocal cord dysfunction familial [MeSH concept]
- vocal cord dysfunction familial [MeSH Supplementary Concept]
Validated automatic mappings to NTBT
- Congenital laryngeal abductor palsy (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients