ODCs

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

PROTEIN INTERACTIONS: 1

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

Feingold syndrome type 1

Melanoma-pancreatic cancer syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MYCN	(0.63)	CDKN2A

Citations in the biomedical literature:

Feingold syndrome type 1		Melanoma-pancreatic cancer syndrome
	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): (no synonyms)

	Classification (Orphanet): - Rare abdominal surgical disease - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Rare gastroenterologic disease - Rare oncologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

	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: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.