Gastrointestinal dysmotility
Symptom Information:
Symptom ID: | HPO:0002579 | ||||
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) Gastrointestinal dysmotility(HPO:0002579) MedDRA: |
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Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Alpers syndrome | (Orphanet:726) |
Behr syndrome | (Orphanet:1239) |
CYCLIC VOMITING SYNDROME | (OMIM:500007) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Fabry disease | (Orphanet:324) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) | (OMIM:613662) |
Megacystis-microcolon-intestinal hypoperistalsis syndrome | (Orphanet:2241) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |