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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
Pelizaeus-Merzbacher-like due to HSPD1 mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Pelizaeus-Merzbacher-like due to HSPD1 mutation

IKBKG
(UniProt - OMIM)
 HSPD1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
IKBKG
(0.72)
HSPD1


Citations in the biomedical literature:


X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
IKBKG
Pelizaeus-Merzbacher-like due to HSPD1 mutation
HSPD1



X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Pelizaeus-Merzbacher-like due to HSPD1 mutation

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):
- Mitochondrial HSP60 chaperonopathy
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.