ODCs

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

PROTEIN INTERACTIONS: 1

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

Alpha-crystallinopathy

Autosomal recessive limb girdle muscular dystrophy type 2A


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CRYAB	(0.63)	CAPN3

Citations in the biomedical literature:

Alpha-crystallinopathy		Autosomal recessive limb girdle muscular dystrophy type 2A
	Synonym(s): - CRYAB-related myofobrillar myopathy		Synonym(s): - LGMD2A - Limb girdle muscular dystrophy due to calpain deficiency - Primary calpainopathy

	Classification (Orphanet): (no data available)		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: 1-9 / 100 000 Average age onset: variable 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.