ODCs

Click node...

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Autosomal recessive limb-girdle muscular dystrophy type 2K

Congenital muscular dystrophy with cerebellar involvement


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	POMT1	(0.55)	POMT2

Citations in the biomedical literature:

Autosomal recessive limb-girdle muscular dystrophy type 2K		Congenital muscular dystrophy with cerebellar involvement
	Synonym(s): - LGMD2K - Limb-girdle muscular dystrophy - intellectual deficit		Synonym(s): - CMD with cerebellar involvement - CMD-CRB

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

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

No signs/symptoms info available.