ODCs

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1 OMIM reference -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Congenital muscular dystrophy, Ullrich type

Autosomal recessive limb-girdle muscular dystrophy type 2B


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL6A3	(0.63)	DYSF

Citations in the biomedical literature:

Congenital muscular dystrophy, Ullrich type		Autosomal recessive limb-girdle muscular dystrophy type 2B
	Synonym(s): - Scleroatonic muscular dystrophy - UCMD - Ullrich disease		Synonym(s): - LGMD2B - Limb-girdle muscular dystrophy due to dysferlin deficiency

	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: Class of prevalence: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: normal Type of inheritance: autosomal recessive

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

No signs/symptoms info available.