ODCs

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

PROTEIN INTERACTIONS: 3

1 associated gene
No signs/symptoms info

Immunodeficiency by defective expression of HLA class 1

Autosomal dominant beta2-microglobulinic amyloidosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TAP1 TAP2 TAPBP	(0.72) (0.63) (0.63)	B2M B2M B2M

Citations in the biomedical literature:

Immunodeficiency by defective expression of HLA class 1		Autosomal dominant beta2-microglobulinic amyloidosis
	Synonym(s): - Bare lymphocyte syndrome type 1		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare immune disease		Classification (Orphanet): - Rare genetic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - 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.