Wheelchair user
Symptom Information:
| Symptom ID: | MedDRA:10047920 | ||
| Synonyms: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
MedDRA: Social circumstances(MedDRA:10041244) Lifestyle issues(MedDRA:10024450) Disability issues(MedDRA:10057171) Wheelchair user(MedDRA:10047920) |
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| Database Frequency: | 3 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Autosomal recessive spastic ataxia with leukoencephalopathy | (Orphanet:314603) |
| Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
| Pyruvate dehydrogenase E2 deficiency | (Orphanet:79244) |