Genes?

Curated: Liver cirrhosis

Unreviewed: N/A

Curated: Cerebellar ataxia, Coenzyme q10 deficiency, Developmental disability, Mitochondrial disease, Spastic ataxia, Primary coenzyme q10 deficiency, Rhabdomyolysis, Ataxia, spastic, autosomal recessive

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, Spinocerebellar Ataxia

Curated: Central nervous system cancer, Coenzyme q10 deficiency, Glioblastoma, Glioma, Intellectual developmental disorder, Mitochondrial disease, Neurodevelopmental disorder, Primary coenzyme q10 deficiency

Unreviewed: Brain disease, Cerebellar ataxia, Cerebellar diseases, Developmental disability, Dysarthria, Growth disorder, Mental retardation, Microcephaly, Myocardial Infarction

Curated: Alzheimer disease, Coenzyme q10 deficiency, Primary coenzyme q10 deficiency, Steroid-resistant nephrotic syndrome

Unreviewed: Atrophy, Coenzyme Q10 Deficiency, Glomerulosclerosis, Hearing Loss, Kidney disease, Nephrotic Syndrome, Neurofibromatosis, Proteinuria, Renal Glomerular Disease, Schwannomatosis, Steroid resistant nephrotic syndrome

Curated: Coenzyme q10 deficiency, Distal hereditary motor neuropathy, Primary coenzyme q10 deficiency, Neuronopathy, distal hereditary motor, autosomal recessive 9

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

Curated: N/A

Unreviewed: N/A

Curated: Autosomal recessive ataxia, Cerebellar ataxia, Cataract, Cerebellar atrophy, Coenzyme q10 deficiency, Congenital neurologic anomalies, Global developmental delay, Gout, Mitochondrial disease, Nystagmus, Spinocerebellar ataxia, Primary coenzyme q10 deficiency

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

Curated: Obstructive pulmonary disease, Crohn disease, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, 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

Curated: Coenzyme q10 deficiency, Leigh syndrome, Mitochondrial disease, Primary coenzyme q10 deficiency

Unreviewed: Brain disease, Cerebellar atrophy, Cerebral Atrophy, Coenzyme Q10 Deficiency, Developmental Delay, Diabetes, Diabetes Mellitus, Encephalopathy-Hypertrophic Cardiomyopathy-Renal Tubular Disease Syndrome, Epileptic encephalopathy, Hyperglycemia, Hyperthyroidism, Hypothyroidism, Inborn Errors Of Metabolism, Lactic acidosis, Left Ventricular Hypertrophy, MERRF Syndrome, Metabolic Diseases, Mitochondrial Diseases, Mitochondrial Electron Transport Chain Deficiencies, Steroid resistant nephrotic syndrome

Curated: N/A

Unreviewed: Amyloidosis, Amyotrophic Lateral Sclerosis, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, Childhood obesity, Colitis, Cone-rod dystrophy, Cystoid macular edema, Hypoxic-Ischemic Encephalopathy, Lateral Sclerosis, Retinitis Pigmentosa