Impaired mitochondrial translation
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 4 / 7739 | |
Resource: |
All diseases associated with this symptom:
Behr syndrome | (Orphanet:1239) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Combined oxidative phosphorylation defect type 9 | (Orphanet:319509) |
MELAS | (Orphanet:550) |