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Brugada syndrome
8 OMIM references -
11 associated genes
51 connected diseases
No signs/symptoms info
Disease Type of connection
Familial progressive cardiac conduction defect
Familial atrial fibrillation
Familial sick sinus syndrome
Romano-Ward syndrome
Timothy syndrome
Atrial stand still
Dravet syndrome
Familial isolated dilated cardiomyopathy
Generalized epilepsy with febrile seizures-plus context
Hypokalemic periodic paralysis
Idiopathic ventricular fibrillation, not Brugada type
Spinocerebellar ataxia type 19 / 22
Catecholaminergic polymorphic ventricular tachycardia
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Congenital analbuminemia
Congenital lethal myopathy, Compton-North type
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
Autosomal dominant limb-girdle muscular dystrophy type 1C
Autosomal dominant spastic paraplegia type 10
Behavioral variant of frontotemporal dementia
Chronic myeloid leukemia
Dehydratase deficiency
Desmoplastic small round cell tumor
Ewing sarcoma
Extraskeletal Ewing sarcoma
Extraskeletal myxoid chondrosarcoma
Greenberg dysplasia
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Isolated CoQ-cytochrome C reductase deficiency
Isolated NADH-CoQ reductase deficiency
Melanoma of soft part
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Progressive non-fluent aphasia
Proximal myotonic myopathy
Reynolds syndrome
Rippling muscle disease
Semantic dementia
Spastic paraplegia - Paget disease of bone
Translocation renal cell carcinoma
X-linked Emery-Dreifuss muscular dystrophy
Cone rod dystrophy
2q37 microdeletion syndrome
Intellectual deficiency - hypotonia - spasticity - sleep disorder
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
X-linked non-syndromic intellectual deficit
- Bangungut
- Dream disease
- Idiopathic ventricular fibrillation, Brugada type
- Pokkuri death syndrome
- Sudden unexplained nocturnal death syndrome

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the circulatory system -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
8 OMIM references -
1 MeSH reference: D053840

No signs/symptoms info available.