Gastroparesis
Symptom Information:
Symptom ID: | HPO:0002578 | |||||||
Synonyms: |
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Quality: | ||||||||
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 stomach(HPO:0002577) Gastroparesis(HPO:0002578) MedDRA: |
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Database Frequency: | 11 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
MELAS | (Orphanet:550) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |
Wolfram syndrome 1 | (OMIM:222300) |