ODCs

Hereditary pheochromocytoma-paraganglioma		Feingold syndrome type 1
	Synonym(s): - Familial pheochromocytoma-paraganglioma - SDHx-related paraganglioma-pheochromocytoma		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

	Classification (Orphanet): - Rare circulatory system disease - Rare endocrine disease - Rare genetic disease - Rare oncologic disease - Rare renal disease		Classification (Orphanet): - Rare abdominal surgical disease - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: adult Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: adult Type of inheritance: autosomal dominant

	External references: 6 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MAX	(0.99)	MYCN