Abnormal mitochondrial shape
Symptom Information:
Symptom ID: | HPO:0012087 | |||||||||||||||||||||||||||||
Synonyms: |
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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 shape(HPO:0012087) MedDRA: Renal and urinary disorders(MedDRA:10038359) Urinary tract signs and symptoms(MedDRA:10046590) Urinary abnormalities(MedDRA:10000196) Abnormal mitochondrial shape(HPO:0012087) |
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Database Frequency: | 8 / 7739 | |||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Barth syndrome | (Orphanet:111) |
Cardiomyopathy, familial restrictive, 3 | (OMIM:612422) |
Cardiomyopathy-hypotonia-lactic acidosis syndrome | (Orphanet:91130) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MELAS | (Orphanet:550) |
MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT | (OMIM:254960) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |