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Distal 17p13.3 microdeletion syndrome

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

6 OMIM references -
6 associated genes
3 signs/symptoms

Distal 17p13.3 microdeletion syndrome

Neuroblastoma

YWHAE	(UniProt - OMIM)		ALK	(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)	YWHAE	(0.73)	TOP2A

Citations in the biomedical literature:

Distal 17p13.3 microdeletion syndrome		Neuroblastoma
	Synonym(s): - Distal del(17)(p13.3 ) - Distal monosomy 17p13.3		Synonym(s): - Neural crest tumor - Sympathoblastoma

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		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
Distal 17p13.3 microdeletion syndrome
(no data available)