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

IKBKG
(UniProt - OMIM)
 RET
(UniProt - OMIM)

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


Citations in the biomedical literature:


X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
IKBKG
Unilateral renal dysplasia
RET



X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Unilateral renal dysplasia

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):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal 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.