2611
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Coenzyme Q10B pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
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2612
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Coenzyme Q2, polyprenyltransferase |
CL640, COQ10D1, MSA1, PHB:PPT |
Curated: Coenzyme q10 deficiency, Focal glomerulosclerosis, Kidney disease, Leigh syndrome, Mitochondrial disease, Multiple system atrophy, Nephrotic syndrome, Shy-drager syndrome, Systemic lupus erythematosus
Unreviewed: Alport Syndrome, Amyotrophic Lateral Sclerosis, Anemia, Anhidrosis, Anxiety Disorder, Bilateral convulsive seizures, Brain disease, Camptocormia, Central Visual Impairment, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar diseases, Cerebral Atrophy, Coenzyme Q10 Deficiency, Developmental regression, Dysarthria, Dysautonomia, Dystonia, Epileptic encephalopathy, Erectile Dysfunction, Female anorgasmia, Focal segmental glomerulosclerosis, Glomerulonephritis, Glomerulosclerosis, Hearing Loss, Hypertrophic cardiomyopathy, Hypoalbuminemia, Hypogonadism, Hypohidrosis, Intestinal Volvulus, Kidney Disease, Kidney failure, Leigh Syndrome With Nephrotic Syndrome, Lissencephaly, Liver failure, Mental Depression, Mental retardation, Metabolic Myopathy, Mitochondrial encephalomyopathy, Motor delay, Multiple System Atrophy, Myoclonic Epilepsy, Myopathy, Myositis, Nephritis, Nephrotic Syndrome, Neurodegenerative Disorders, Neuromuscular Diseases, Neuromuscular dysphagia, Nystagmus, Olivopontocerebellar Atrophies, Optic atrophy, Orofacial dyskinesia, Orthostatic syncope, Pancytopenia, Parkinson disease, Ptosis, Raynaud Phenomenon, Renal cyst, Renal Glomerular Disease, Rod-cone dystrophy, Senior-loken syndrome, Sleep Apnea, Specific Learning Disorder, Spinocerebellar Ataxia, Steroid resistant nephrotic syndrome, Striatonigral Degeneration
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2613
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|
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Coenzyme Q3, methyltransferase |
DHHBMT, DHHBMTASE, UG0215E05, bA9819.1 |
Curated: Liver cirrhosis
Unreviewed: N/A
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2614
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|
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Coenzyme Q4 |
CGI-92, COQ10D7, SPAX10 |
Curated: Cerebellar ataxia, Coenzyme q10 deficiency, Developmental disability, Mitochondrial disease, Spastic ataxia
Unreviewed: Ataxia, Brain disease, Cardiomyopathy, Coenzyme Q10 Deficiency, Dysmorphic Features, Dysphagia, Encephalomyopathy-Cardiomyopathy-Respiratory Distress Syndrome, Epilepsy, Epileptic encephalopathy, Hypotonia, Intellectual developmental disorder, Leigh Syndrome, Mental retardation, Metabolic syndrome, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Multiple Congenital Anomalies, Rhabdomyolysis, Spinocerebellar Ataxia
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2615
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|
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Coenzyme Q5, methyltransferase |
COQ10D9 |
Curated: Central nervous system cancer, Coenzyme q10 deficiency, Glioblastoma, Glioma, Intellectual developmental disorder, Mitochondrial disease, Neurodevelopmental disorder
Unreviewed: Brain disease, Cerebellar ataxia, Cerebellar diseases, Developmental disability, Dysarthria, Growth disorder, Mental retardation, Microcephaly, Myocardial Infarction
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2616
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|
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Coenzyme Q6, monooxygenase |
CGI-10, CGI10, COQ10D6 |
Curated: Alzheimer disease, Coenzyme q10 deficiency, Primary coenzyme q10 deficiency
Unreviewed: Atrophy, Coenzyme Q10 Deficiency, Glomerulosclerosis, Hearing Loss, Kidney disease, Nephrotic Syndrome, Neurofibromatosis, Proteinuria, Renal Glomerular Disease, Schwannomatosis, Steroid resistant nephrotic syndrome
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2617
|
|
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Coenzyme Q7, hydroxylase |
CAT5, CLK-1, CLK1, COQ10D8, HMNR9 |
Curated: Coenzyme q10 deficiency, Coq7-related distal hereditary motor neuropathy, Distal hereditary motor neuropathy, Primary coenzyme q10 deficiency
Unreviewed: Coenzyme Q10 Deficiency, Developmental Delay, Developmental disability, Hypertension, Intracranial Aneurysm, Left Ventricular Hypertrophy, Mitochondrial complex deficiency, Mitochondrial disease, Motor delay, Nervous system disease, Neurodegenerative Disorders, Polyneuropathy, Pulmonary hypoplasia, Renal dysplasia, Steroid resistant nephrotic syndrome
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2618
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|
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COQ7 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
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2619
|
|
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Coenzyme Q8A |
ADCK3, ARCA2, CABC1, COQ10D4, COQ8, SCAR9 |
Curated: Autosomal recessive ataxia, Cerebellar ataxia, Cataract, Cerebellar atrophy, Coenzyme q10 deficiency, Congenital neurologic anomalies, Global developmental delay, Gout, Mitochondrial disease, Nystagmus, Spinocerebellar ataxia
Unreviewed: Anxiety Disorder, Ataxia, Ataxia telangiectasia, Cerebellar Ataxia, Cerebellar diseases, Coenzyme Q10 Deficiency, Cognition disorder, Dementia, Developmental regression, Dystonia, Endometrial neoplasm, Epilepsy, Epileptic encephalopathy, Friedreich Ataxia, Gynecomastia, Kearns Sayre Syndrome, Leigh Syndrome, Marinesco-Sjogren Syndrome, MELAS Syndrome, Mental Disorders, Mental retardation, MERRF Syndrome, Mitochondrial Diseases, Mitochondrial encephalopathy, Nephrotic syndrome, Scoliosis, Seizures, Spastic Ataxia, Spinocerebellar Ataxia, Strabismus, Stroke, Vacuolar myopathy
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2620
|
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Coenzyme Q8B |
ADCK4, NPHS9 |
Curated: Obstructive pulmonary disease, Crohn disease, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Inflammatory bowel disease, Mitochondrial disease, Kawasaki disease, Nephrotic syndrome, Retinitis pigmentosa, Ulcerative colitis
Unreviewed: Alport Syndrome, Aortic Aneurysm, Coenzyme Q10 Deficiency, Genetic Steroid-Resistant Nephrotic Syndrome, Glomerulosclerosis, Hypoalbuminemia, Intellectual developmental disorder, Kidney Disease, Kidney Failure, Medullary nephrocalcinosis, Nephritis, Nephrosis, Congenital, Nephrotic Syndrome, Ovarian neoplasm, Polycystic kidney disease, Proteinuria, Renal Glomerular Disease, Renal glycosuria, Retinitis Pigmentosa, Seizures, Steroid resistant nephrotic syndrome, Thoracic aortic aneurysm
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