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Neurofibromatosis type 3
3 OMIM references -
3 associated genes
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
Neurofibromatosis type 3
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency

LZTR1
(UniProt - OMIM)
 IKBKG
(UniProt - OMIM)
NF2
(UniProt - OMIM)
SMARCB1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LZTR1
(0.63)
IKBKG


Citations in the biomedical literature:


Neurofibromatosis type 3
LZTR1 NF2 SMARCB1
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
IKBKG



Neurofibromatosis type 3
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency

Synonym(s):
- NF3
- Neurilemmomatosis
- Schwannomatosis
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
- Rare oncologic disease
- Rare skin 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:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
3 OMIM references -
1 MeSH reference: C536641
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.