Mitochondrial DNA deletion

Symptom Information:

Symptom ID: MedDRA:10051403
Synonyms:
Mitochondrial DNA deletion (1 patient) [OMIM:Mitochondrial DNA deletion (1 patient)]
Mitochondrial DNA deletions [OMIM:Mitochondrial DNA deletions]
Mitochondrial DNA deletions (in some patients) [OMIM:Mitochondrial DNA deletions (in some patients)]
Quality:
Cross references:
OMIM: "Mitochondrial DNA deletion (1 patient)" [OMIM:Mitochondrial DNA deletion (1 patient)]
OMIM: "Mitochondrial DNA deletions" [OMIM:Mitochondrial DNA deletions]
OMIM: "Mitochondrial DNA deletions (in some patients)" [OMIM:Mitochondrial DNA deletions (in some patients)]
Is a (Direct Parents):
MedDRA Cell metabolism disorders NEC
Is a (Whole tree): HPO:
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Metabolism disorders NEC(MedDRA:10000546)
       Cell metabolism disorders NEC(MedDRA:10057187)
          Mitochondrial DNA deletion(MedDRA:10051403)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant limb-girdle muscular dystrophy type 1H (Orphanet:238755)
Autosomal dominant optic atrophy and congenital deafness (Orphanet:3212)
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY (OMIM:614520)
Kearns-Sayre syndrome (Orphanet:480)
MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE) (OMIM:615418)
Progressive external ophthalmoplegia - myopathy - emaciation (Orphanet:352447)