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Feingold syndrome type 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

6 OMIM references -
6 associated genes
3 signs/symptoms

Feingold syndrome type 1

Neuroblastoma

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


COMMON GENES	MYCN

Citations in the biomedical literature:

Feingold syndrome type 1		Neuroblastoma
	Synonym(s): - Brunner-Winter syndrome type 1 - Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1 - FGLDS1 - FS1 - MMT type 1 - MODED syndrome type 1 - Microcephaly - intellectual deficit - tracheoesophageal fistula type 1 - Microcephaly - oculo-digito-esophageal-duodenal syndrome type 1 - Microcephaly-digital anomalies-normal intelligence type 1 - ODED syndrome type 1 - Oculo-digito-esophageal-duodenal syndrome type 1		Synonym(s): - Neural crest tumor - Sympathoblastoma

	Classification (Orphanet): - Rare abdominal surgical disease - Rare bone disease - 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: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: adult Type of inheritance: autosomal dominant		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: 1 OMIM reference - 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
Feingold syndrome type 1
(no data available)