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6 OMIM references -
6 associated genes
3 signs/symptoms

PROTEIN INTERACTIONS: 1

Atypical Werner syndrome

1 associated gene
No signs/symptoms info

Neuroblastoma

Atypical Werner syndrome

ALK	(UniProt - OMIM)		LMNA	(UniProt - OMIM)
HACE1	(UniProt - OMIM)
LIN28B	(UniProt - OMIM)
MYCN	(UniProt - OMIM)
PHOX2B	(UniProt - OMIM)
TOP2A	(UniProt - OMIM)


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

Citations in the biomedical literature:

Neuroblastoma		Atypical Werner syndrome
	Synonym(s): - Neural crest tumor - Sympathoblastoma		Synonym(s): - Atypical progeroid syndrome

	Classification (Orphanet): - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease

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

	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: No OMIM references No MeSH references

Neuroblastoma
	Very frequent - Central nervous system / peripheral nerves neoplasm / tumor / carcinoma / cancer - Organic acid metabolism anomalies Frequent - Autosomal dominant inheritance
Atypical Werner syndrome
(no data available)