Muscle biopsy shows mitochondrial paracrystalline inclusions
Symptom Information:
|
Symptom ID:
|
OMIM : No Id available
|
|
Synonyms:
|
|
|
Quality:
|
|
|
Cross references:
|
| OMIM: "Muscle biopsy shows mitochondrial paracrystalline inclusions" [OMIM:Muscle biopsy shows mitochondrial paracrystalline inclusions] |
|
|
Is a (Direct Parents):
|
|
|
Is a (Whole tree):
|
HPO:
MedDRA:
|
|
Database Frequency:
|
2 / 7739
|
|
Resource:
|
|
All diseases associated with this symptom:
|
Glycogen storage disease due to muscle phosphorylase kinase deficiency
|
(Orphanet:715)
|
|
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
|
(Orphanet:324525)
|