ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

6 associated genes
No signs/symptoms info

Multiple paragangliomas associated with polycythemia

Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EPAS1	(0.68)	NDN

Citations in the biomedical literature:

Multiple paragangliomas associated with polycythemia		Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
	Synonym(s): - Multiple paragangliomas associated with erythrocytosis - Paraganglioma - somatostatinoma - polycythemia		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare endocrine disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare infertility - Rare neurologic disease

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: sporadic		Epidemiological data: (no data available)

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.