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Familial isolated hyperparathyroidism
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute necrotizing encephalopathy of childhood
1 OMIM reference -
2 associated genes
No signs/symptoms info
Familial isolated hyperparathyroidism
Acute necrotizing encephalopathy of childhood

CDC73
(UniProt - OMIM)
 CPT2
(UniProt - OMIM)
MEN1
(UniProt - OMIM)
 RANBP2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CDC73
(0.72)
RANBP2


Citations in the biomedical literature:


Familial isolated hyperparathyroidism
CDC73 MEN1
Acute necrotizing encephalopathy of childhood
CPT2 RANBP2



Familial isolated hyperparathyroidism
Acute necrotizing encephalopathy of childhood

Synonym(s):
- FIHPT
Synonym(s):
- ANEC
- Isolated ANE
- Isolated acute necrotizing encephalopathy
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare infectious disease
- Rare neurologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.