ODCs

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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

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation


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

Citations in the biomedical literature:

Neuroblastoma		Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
	Synonym(s): - Neural crest tumor - Sympathoblastoma		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Neoplasms -		Classification (ICD10): (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		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	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
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
(no data available)