Cytoscape Web
Click node...

Autosomal recessive lymphoproliferative disease
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal recessive lymphoproliferative disease
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency

CD27
(UniProt - OMIM)
 IKBKG
(UniProt - OMIM)
ITK
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ITK
(0.68)
IKBKG


Citations in the biomedical literature:


Autosomal recessive lymphoproliferative disease
CD27 ITK
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
IKBKG



Autosomal recessive lymphoproliferative disease
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- X-linked MSMD due to IKBKG deficiency
- X-linked MSMD due to NEMO deficiency
- X-linked mendelian susceptibility to mycobacterial diseases due to NEMO deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare oncologic 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: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.