ODCs

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

PROTEIN INTERACTIONS: 2

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

Alpha-crystallinopathy

Hemoglobin H disease

CRYAB	(UniProt - OMIM)		HBA1	(UniProt - OMIM)
			HBA2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CRYAB CRYAB	(0.56) (0.56)	HBA1 HBA2

Citations in the biomedical literature:

Alpha-crystallinopathy		Hemoglobin H disease
	Synonym(s): - CRYAB-related myofobrillar myopathy		Synonym(s): - Alpha-thalassemia intermedia - HbH disease

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare hematologic disease - Rare renal disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: variable Average age of death: - 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.