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6 OMIM references -
9 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
8 OMIM references -
11 associated genes
No signs/symptoms info
Isolated CoQ-cytochrome C reductase deficiency
Brugada syndrome

BCS1L CACNA1C
CYC1 CACNB2
LYRM7 GPD1L
MT-CYB HCN4
TTC19 KCND3
UQCC2 KCNE3
UQCRB KCNJ8
UQCRC2 SCN1B
UQCRQ SCN3B
SCN5A
TRPM4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
UQCRC2
(0.63)
KCND3



Citations in the biomedical literature:


Isolated CoQ-cytochrome C reductase deficiency
BCS1L CYC1 LYRM7 MT-CYB TTC19 UQCC2
UQCRB UQCRC2 UQCRQ
Brugada syndrome
CACNA1C CACNB2 GPD1L HCN4 KCND3 KCNE3
KCNJ8 SCN1B SCN3B SCN5A TRPM4



Isolated CoQ-cytochrome C reductase deficiency
Brugada syndrome

Synonym(s):
- Isolated coenzyme Q-cytochrome C reductase deficiency
- Isolated mitochondrial respiratory chain complex III deficiency
- Isolated ubiquinone-cytochrome C reductase deficiency

Synonym(s):
- Bangungut
- Dream disease
- Idiopathic ventricular fibrillation, Brugada type
- Pokkuri death syndrome
- SUNDS
- Sudden unexplained nocturnal death syndrome

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease

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

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
6 OMIM references -
No MeSH references
External references:
8 OMIM references -
1 MeSH reference: D053840

No signs/symptoms info available.