ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency

Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	IL12B	(0.69)	IL12RB1

Citations in the biomedical literature:

Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency		Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
	Synonym(s): - MSMD due to complete IL12B deficiency - MSMD due to complete interleukin 12B deficiency - Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency		Synonym(s): - MSMD due to complete IL12RB1 deficiency - MSMD due to complete interleukin 12 receptor beta 1 deficiency - Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency

	Classification (Orphanet): - Rare genetic disease - Rare immune disease		Classification (Orphanet): - Rare genetic disease - Rare immune disease

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: adult Type of inheritance: autosomal recessive

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

No signs/symptoms info available.