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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Intermittent hydrarthrosis
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency

MEFV IKBKG
TNFRSF1A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TNFRSF1A
(0.83)
IKBKG



Citations in the biomedical literature:


Intermittent hydrarthrosis
MEFV TNFRSF1A
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
IKBKG



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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.