Genetic mitochondrial abnormalities NEC

Symptom Information:

Symptom ID: MedDRA:10052637
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
MedDRA Cytoplasmic disorders congenital
Is a (Whole tree): HPO:
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Cytoplasmic disorders congenital(MedDRA:10052635)
       Genetic mitochondrial abnormalities NEC(MedDRA:10052637)
Database Frequency: 0 / 7739
Resource:

All diseases associated with this symptom: