Malnutrition
Symptom Information:
| Symptom ID: | HPO:0004395 | ||||
| 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) Abdominal symptom(HPO:0011458) Malnutrition(HPO:0004395) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Appetite and general nutritional disorders(MedDRA:10003018) General nutritional disorders NEC(MedDRA:10018067) Malnutrition(HPO:0004395) |
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| Database Frequency: | 12 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Chylomicron retention disease | (Orphanet:71) |
| Familial visceral myopathy | (Orphanet:2604) |
| Hereditary fructose intolerance | (Orphanet:469) |
| Isolated congenital hypoglossia/aglossia | (Orphanet:141152) |
| Lysinuric protein intolerance | (Orphanet:470) |
| MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) | (OMIM:613662) |
| Microvillous inclusion disease | (Orphanet:2290) |
| Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
| Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
| Pancreatic insufficiency - anemia - hyperostosis | (Orphanet:199337) |
| Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
| Tropical endomyocardial fibrosis | (Orphanet:75565) |