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Myosclerosis
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Bethlem myopathy
Congenital muscular dystrophy, Ullrich type
Fibronectin glomerulopathy
Synonym(s):
- Congenital myosclerosis, Löwenthal type
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
COL6A2 P12110120240
No signs/symptoms info available.