vocal cord dysfunction familial

Preferred Label : vocal cord dysfunction familial;

MeSH synonym : plott syndrome; laryngeal abductor paralysis; familial vocal cord dysfunction; gerhardt syndrome; vocal cord dysfunction, familial;

Is substance : O;

Détails

Origin ID

C536354;

UMLS CUI

C0396059;

Automatic exact mappings (from CISMeF team)
- Laryngeal adductor paralysis [OMIM Phenotype]
Currated CISMeF NLP mapping
- Congenital laryngeal abductor palsy (disorder) [SNOMED CT concept]
- Laryngeal abductor paralysis [ICD-11 More detail]
- Laryngeal abductor paralysis [OMIM Phenotype]
- Laryngeal abductor paralysis [ORDO Disease]
- Laryngeal abductor paralysis, X-linked [OMIM Phenotype]
- Laryngeal abductor paralysis-intellectual disability syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- vocal cord paralysis [MeSH Descriptor]
Record concept(s)
- Vocal cord dysfunction familial [MeSH concept]
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 [OMIM Phenotype]
- Laryngeal abductor paralysis [ORDO Disease]
- Laryngeal abductor paralysis, X-linked [OMIM Phenotype]
- Laryngeal abductor paralysis-intellectual disability syndrome [ORDO Disease]
Validated automatic mappings to BTNT
- Laryngeal abductor paralysis with intellectual disability syndrome (disorder) [SNOMED CT concept]

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