ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

2 OMIM references -
4 associated genes
No signs/symptoms info

Autosomal recessive limb-girdle muscular dystrophy type 2M

Congenital muscular dystrophy without intellectual disability

Citations in the biomedical literature:

Autosomal recessive limb-girdle muscular dystrophy type 2M		Congenital muscular dystrophy without intellectual disability
	Synonym(s): - LGMD2M		Synonym(s): - CMD without intellectual disability - CMD-no MR

	Classification (Orphanet): - Inborn errors of metabolism - Rare cardiac disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.