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2 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial isolated hyperparathyroidism
Hyperparathyroidism - jaw tumor syndrome

CDC73 CDC73
MEN1


COMMON
GENES
CDC73



Citations in the biomedical literature:


Familial isolated hyperparathyroidism
CDC73 MEN1
Hyperparathyroidism - jaw tumor syndrome



Familial isolated hyperparathyroidism
Hyperparathyroidism - jaw tumor syndrome

Synonym(s):
- FIHPT

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

No signs/symptoms info available.