ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

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

Familial parathyroid adenoma

Hyperparathyroidism - jaw tumor syndrome

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

Citations in the biomedical literature:

Familial parathyroid adenoma		Hyperparathyroidism - jaw tumor syndrome
	Synonym(s): (no synonyms)		Synonym(s): - HPT-JT

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

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

	Epidemiological data: (no data available)		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.