Abnormal mitochondrial number
Symptom Information:
Symptom ID: | HPO:0012102 | ||||||
Synonyms: |
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Quality: | |||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of cell physiology(HPO:0011017) Abnormality of the mitochondrion(HPO:0012103) Abnormal mitochondrial morphology(HPO:0008322) Abnormal mitochondrial number(HPO:0012102) MedDRA: |
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Database Frequency: | 4 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Recessive mitochondrial ataxia syndrome | (Orphanet:94125) |