velopharyngeal insufficiency

Preferred Label : velopharyngeal insufficiency;

UMLS semantic type : T019 - Congenital Abnormality; T020 - Acquired Abnormality;

Origin ID

M0022583;

UMLS CUI

C0042454;

Automatic exact mappings (from CISMeF team)
- Velopharyngeal insufficiency [PASCAL descriptor]
Currated CISMeF NLP mapping
- Palatopharyngeal incompetence [OMIM Phenotype]
- Velopharyngeal inadequacy (disorder) [SNOMED CT concept]
- Velopharyngeal incompetence [MedDRA Preferred Term]
- Velopharyngeal incompetence (disorder) [SNOMED CT concept]
- Velopharyngeal insufficiency [HPO term]
- Velopharyngeal insufficiency (disorder) [SNOMED CT concept]
Related record
- velopharyngeal insufficiency [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Palatopharyngeal incompetence [OMIM Phenotype]
- Velopharyngeal inadequacy (disorder) [SNOMED CT concept]
- Velopharyngeal incompetence [MedDRA Preferred Term]
- Velopharyngeal incompetence (disorder) [SNOMED CT concept]
- Velopharyngeal insufficiency [HPO term]
- Velopharyngeal insufficiency (disorder) [SNOMED CT concept]