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Isolated CoQ-cytochrome C reductase deficiency
6 OMIM references -
9 associated genes
68 connected diseases
No signs/symptoms info
Disease Type of connection
Histiocytoid cardiomyopathy
Leber hereditary optic neuropathy
Leigh syndrome with nephrotic syndrome
Björnstad syndrome
GRACILE syndrome
Renal tubulopathy - encephalopathy - liver failure
Isolated NADH-CoQ reductase deficiency
Leigh syndrome with leukodystrophy
Huntington disease
Juvenile Huntington disease
CLN3 disease
Precursor T-cell acute lymphoblastic leukemia
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Blackfan-Diamond anemia
Fatal infantile cytochrome C oxidase deficiency
Leigh syndrome with cardiomyopathy
Autosomal thrombocytopenia with normal platelets
X-linked intellectual deficit with marfanoid habitus
X-linked non-syndromic intellectual deficit
Burkitt lymphoma
Alternating hemiplegia of childhood
Benign paroxysmal torticollis of infancy
Familial or sporadic hemiplegic migraine
Familial paroxysmal ataxia
Spinocerebellar ataxia type 6
Acute basophilic leukemia
Autosomal agammaglobulinemia
Autosomal recessive limb-girdle muscular dystrophy type 2G
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Behçet disease
Brugada syndrome
Cockayne syndrome type 1
Cockayne syndrome type 2
Cockayne syndrome type 3
Cowden syndrome
Craniometaphyseal dysplasia
Familial isolated dilated cardiomyopathy
Hermansky-Pudlak syndrome without pulmonary fibrosis
Hypoplastic left heart syndrome
Immunodeficiency due to an early component of complement deficiency
Legius syndrome
Oculodentodigital dysplasia
Parkinsonian-pyramidal syndrome
Precursor B-cell acute lymphoblastic leukemia
Proteus syndrome
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 19 / 22
Syndactyly type 3
UV-sensitive syndrome
Wolf-Hirschhorn syndrome
X-linked distal arthrogryposis multiplex congenita
Young adult-onset Parkinsonism
Amyotrophic lateral sclerosis
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Isolated ATP synthase deficiency
Immunodeficiency by defective expression of HLA class 1
Ketoacidosis due to beta-ketothiolase deficiency
Postaxial acrofacial dysostosis
Pyruvate dehydrogenase E3 deficiency
SURF1-related Charcot-Marie-Tooth disease type 4
- Isolated coenzyme Q-cytochrome C reductase deficiency
- Isolated mitochondrial respiratory chain complex III deficiency
- Isolated ubiquinone-cytochrome C reductase deficiency

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic 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:
6 OMIM references -
No MeSH references

No signs/symptoms info available.