ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

4 associated genes
No signs/symptoms info

Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency

Pediatric systemic lupus erythematosus


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	IFNGR1	(0.63)	STAT4

Citations in the biomedical literature:

Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency		Pediatric systemic lupus erythematosus
	Synonym(s): - Autosomal dominant MSMD due to partial IFNgammaR1 deficiency - Autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency - Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency		Synonym(s): - SLE, pediatric onset

	Classification (Orphanet): - Rare genetic disease - Rare immune disease		Classification (Orphanet): - Rare neurologic disease - Rare renal disease - Rare respiratory 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): - Diseases of the musculoskeletal system and connective tissue -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.