Abnormal mitochondrial morphology

Symptom Information:

Symptom ID: HPO:0008322
Abnormal mitochondrion morphology [HPO:0008322]
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the mitochondrion
Is a (Whole tree): HPO:
    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)
Database Frequency: 8 / 7739

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)