Encephalomyopathy
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 2 / 7739 | |
Resource: |
All diseases associated with this symptom:
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |