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Familial short QT syndrome
3 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial isolated hyperparathyroidism
2 OMIM references -
2 associated genes
No signs/symptoms info
Familial short QT syndrome
Familial isolated hyperparathyroidism

CACNA2D1
(UniProt - OMIM)
 CDC73
(UniProt - OMIM)
KCNH2
(UniProt - OMIM)
 MEN1
(UniProt - OMIM)
KCNJ2
(UniProt - OMIM)
KCNQ1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KCNH2
(0.63)
CDC73


Citations in the biomedical literature:


Familial short QT syndrome
CACNA2D1 KCNH2 KCNJ2 KCNQ1
Familial isolated hyperparathyroidism
CDC73 MEN1



Familial short QT syndrome
Familial isolated hyperparathyroidism

Synonym(s):
- SQTS
Synonym(s):
- FIHPT
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
3 OMIM references -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.