Abnormal mitochondria in muscle tissue

Symptom Information:

Symptom ID: HPO:0008316
Synonyms:
Abnormal mitochondria in muscle [HPO:0008316]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of mitochondrial metabolism
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)
                Abnormality of mitochondrial metabolism(HPO:0003287)
                   Abnormal mitochondria in muscle tissue(HPO:0008316)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Hereditary myopathy with lactic acidosis due to ISCU deficiency (Orphanet:43115)
Isolated NADH-CoQ reductase deficiency (Orphanet:2609)
Isolated succinate-CoQ reductase deficiency (Orphanet:3208)
OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA (OMIM:258470)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)