ODCs

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6 OMIM references -
7 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Hereditary pheochromocytoma-paraganglioma

Carcinoid tumor and carcinoid syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SDHC	(0.59)	SDHD

Citations in the biomedical literature:

Hereditary pheochromocytoma-paraganglioma		Carcinoid tumor and carcinoid syndrome
	Synonym(s): - Familial pheochromocytoma-paraganglioma - SDHx-related paraganglioma-pheochromocytoma		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare circulatory system disease - Rare endocrine disease - Rare genetic disease - Rare oncologic disease - Rare renal disease		Classification (Orphanet): - Rare endocrine disease - Rare gastroenterologic disease - Rare oncologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	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: (no data available)

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

No signs/symptoms info available.