ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Alpha-crystallinopathy

Alexander disease type II


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CRYAB	(0.56)	GFAP

Citations in the biomedical literature:

Alpha-crystallinopathy		Alexander disease type II
	Synonym(s): - CRYAB-related myofobrillar myopathy		Synonym(s): - AxD type II

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: adult Type of inheritance: autosomal dominant

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

No signs/symptoms info available.