Velopharyngeal insufficiency

Symptom Information:

Symptom ID: HPO:0000220
Synonyms:
Velopharyngeal incompetence [HPO:0000220]
Velopharyngeal insufficiency (disorder) [Orphanet:26020]
Velopharyngeal inadequacy (disorder) [Orphanet:26020]
Velopharyngeal incompetence (disorder) [Orphanet:26020]
Velopharyngeal Insufficiency [Orphanet:26020]
Velopharyngeal incompetence [OMIM:Velopharyngeal incompetence]
Velopharyngeal insufficiency [OMIM:Velopharyngeal insufficiency]
Respiratory-digestive intersection/aero-digestive cross-roads anomaly [Orphanet:26020]
Velopharyngeal incompetence [Orphanet:26020]
Velopharyngeal incompetence [MedDRA:10066790]
Quality:
Cross references:
Orphanet:26020 "Respiratory-digestive intersection/aero-digestive cross-roads anomaly" [Orphanet:26020]
OMIM: "Velopharyngeal incompetence" [OMIM:Velopharyngeal incompetence]
OMIM: "Velopharyngeal insufficiency" [OMIM:Velopharyngeal insufficiency]
UMLS:C0042454 "Velopharyngeal Insufficiency" [Orphanet:26020]
Is a (Direct Parents):
HPO         Abnormality of the soft palate
MedDRA Pharyngeal disorders (excl infections and neoplasms)
Orphanet Structural anomalies of the digestive tract
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the palate(HPO:0000174)
                         Abnormality of the soft palate(HPO:0100736)
                            Velopharyngeal insufficiency(HPO:0000220)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Upper respiratory tract disorders (excl infections)(MedDRA:10046304)
       Pharyngeal disorders (excl infections and neoplasms)(MedDRA:10034823)
          Velopharyngeal insufficiency(HPO:0000220)
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 microduplication syndrome (Orphanet:1727)
Adducted thumbs - arthrogryposis, Christian type (Orphanet:2952)
Congenital velopharyngeal incompetence (Orphanet:2291)
Dubowitz syndrome (Orphanet:235)
Hypomandibular faciocranial dysostosis (Orphanet:1790)
Mowat-Wilson syndrome (Orphanet:2152)
Nager syndrome (Orphanet:245)
RAPP-HODGKIN SYNDROME (OMIM:129400)
Smith-Magenis syndrome (Orphanet:819)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)