Mitochondrial DNA deletion
Symptom Information:
Symptom ID: | MedDRA:10051403 | |||
Synonyms: |
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Is a (Direct Parents): |
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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) |
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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) |