ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Familial isolated hyperparathyroidism

Zollinger-Ellison syndrome

CDC73	(UniProt - OMIM)		MEN1	(UniProt - OMIM)
MEN1	(UniProt - OMIM)

Citations in the biomedical literature:

Familial isolated hyperparathyroidism		Zollinger-Ellison syndrome
	Synonym(s): - FIHPT		Synonym(s): - Gastrinoma

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: normal Type of inheritance: sporadic

	External references: 2 OMIM references - No MeSH references		External references: No OMIM references 2 MeSH references: D015043 / D015408

No signs/symptoms info available.