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Lissencephaly due to TUBA1A mutation
1 OMIM reference -
1 associated gene
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
Lissencephaly due to TUBA1A mutation
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency

TUBA1A
(UniProt - OMIM)
 IKBKG
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TUBA1A
(0.72)
IKBKG


Citations in the biomedical literature:


Lissencephaly due to TUBA1A mutation
TUBA1A
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
IKBKG



Lissencephaly due to TUBA1A mutation
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 developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.