Spontaneous esophageal perforation
Symptom Information:
Symptom ID: | HPO:0005203 | |||
Synonyms: |
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Cross references: |
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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) Spontaneous esophageal perforation(HPO:0005203) MedDRA: |
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Database Frequency: | 2 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |