Oral-pharyngeal dysphagia
Symptom Information:
Symptom ID: | HPO:0200136 | ||||
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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 the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Abnormality of the esophagus(HPO:0002031) Dysphagia(HPO:0002015) Oral-pharyngeal dysphagia(HPO:0200136) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the pharynx(HPO:0000600) Oral-pharyngeal dysphagia(HPO:0200136) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Dysphagia(HPO:0002015) Oral-pharyngeal dysphagia(HPO:0200136) MedDRA: |
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Database Frequency: | 1 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
17p11.2 microduplication syndrome | (Orphanet:1713) |