Abnormal mitochondrial morphology
Symptom Information:
| Symptom ID: | HPO:0008322 | ||
| Synonyms: |
|
||
| Quality: | |||
| Cross references: |
|
||
| Is a (Direct Parents): |
|
||
| 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) MedDRA: |
||
| Database Frequency: | 8 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Barth syndrome | (Orphanet:111) |
| Combined oxidative phosphorylation defect type 17 | (Orphanet:369913) |
| Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
| Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
| Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
| MELAS | (Orphanet:550) |
| Maternally-inherited Leigh syndrome | (Orphanet:255210) |
| Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |