Mitochondrial DNA depletion
Symptom Information:
Symptom ID: | MedDRA:10059396 | |||
Synonyms: |
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Cross references: |
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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 depletion(MedDRA:10059396) |
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Database Frequency: | 5 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Alpers syndrome | (Orphanet:726) |
Fatal infantile lactic acidosis with methylmalonic aciduria | (Orphanet:17) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |