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Moderate multiminicore disease with hand involvement
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Benign Samaritan congenital myopathy
1 associated gene
No signs/symptoms info
Moderate multiminicore disease with hand involvement
Benign Samaritan congenital myopathy

RYR1
(UniProt - OMIM)
 RYR1
(UniProt - OMIM)

COMMON
GENES 		RYR1


Citations in the biomedical literature:


Moderate multiminicore disease with hand involvement
RYR1
Benign Samaritan congenital myopathy



Moderate multiminicore disease with hand involvement
Benign Samaritan congenital myopathy

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.