Abnormality of the mitochondrion
Symptom Information:
Symptom ID: | HPO:0012103 | ||
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) MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Arrhythmogenic right ventricular dysplasia, familial, 6 | (OMIM:604401) |
Barth syndrome | (Orphanet:111) |
Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
Nephronophthisis-like nephropathy 1 | (OMIM:613159) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
Ramsay-Hunt syndrome | (Orphanet:3020) |