ODCs

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5 OMIM references -
5 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Congenital muscular dystrophy with intellectual disability

Autosomal recessive limb-girdle muscular dystrophy type 2I

Citations in the biomedical literature:

Congenital muscular dystrophy with intellectual disability		Autosomal recessive limb-girdle muscular dystrophy type 2I
	Synonym(s): - CMD with intellectual disability - CMD-MR		Synonym(s): - LGMD2I - Limb girdle muscular dystrophy due to FKRP deficiency

	Classification (Orphanet): - Inborn errors of metabolism - 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: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: childhood Average age of death: no data available Type of inheritance: autosomal recessive

	External references: 5 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.