Cytoscape Web
Click node...

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

IKBKG
(UniProt - OMIM)
 TBC1D7
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
IKBKG
(0.68)
TBC1D7


Citations in the biomedical literature:


X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
IKBKG
Isolated megalencephaly
TBC1D7



X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Isolated megalencephaly

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
Synonym(s):
- Isolated macrencephaly
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare neurologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.