Velopharyngeal insufficiency
Symptom Information:
Symptom ID: | HPO:0000220 | ||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) |
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Database Frequency: | 10 / 7739 | ||||||||||
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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) |