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Isolated succinate-CoQ reductase deficiency
1 OMIM reference -
4 associated genes
7 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary pheochromocytoma-paraganglioma
Carney-Stratakis syndrome
Cowden syndrome
Gastrointestinal stromal tumor
Carcinoid tumor and carcinoid syndrome
Familial isolated dilated cardiomyopathy
Leigh syndrome with leukodystrophy
Synonym(s):
- Isolated mitochondrial respiratory chain complex II deficiency
- Isolated succinate-coenzyme Q reductase deficiency
- Isolated succinate-ubiquinone reductase deficiency
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SDHA P31040600857
SDHAF1 A6NFY7612848
SDHB P21912185470
SDHD O14521602690
No signs/symptoms info available.