Impaired mitochondrial translation

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Impaired mitochondrial translation" [OMIM:Impaired mitochondrial translation]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
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)