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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 OMIM references -
6 associated genes
3 signs/symptoms
Laminopathy type Decaudain-Vigouroux
Neuroblastoma

LMNA ALK
HACE1
LIN28B
MYCN
PHOX2B
TOP2A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.49)
TOP2A



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Neuroblastoma
ALK HACE1 LIN28B MYCN PHOX2B TOP2A



Laminopathy type Decaudain-Vigouroux
Neuroblastoma

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

Synonym(s):
- Neural crest tumor
- Sympathoblastoma

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Neoplasms -

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

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

Neuroblastoma

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

Frequent
- Autosomal dominant inheritance



Laminopathy type Decaudain-Vigouroux

(no data available)