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6 OMIM references -
6 associated genes
3 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Neuroblastoma
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency

ALK IKBKG
HACE1
LIN28B
MYCN
PHOX2B
TOP2A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ALK
(0.56)
IKBKG



Citations in the biomedical literature:


Neuroblastoma
ALK HACE1 LIN28B MYCN PHOX2B TOP2A

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



Neuroblastoma
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency

Synonym(s):
- Neural crest tumor
- Sympathoblastoma

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 neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: childhood
Average age of death: child / adolescent
Type of inheritance: sporadic
Epidemiological data:
(no data available)

External references:
6 OMIM references -
2 MeSH references: C536408 / D009447
External references:
1 OMIM reference -
No MeSH references

Neuroblastoma

Very frequent
- Central nervous system / peripheral nerves neoplasm / tumor / carcinoma / cancer
- Organic acid metabolism anomalies

Frequent
- Autosomal dominant inheritance



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

(no data available)