191
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Acyl-CoA dehydrogenase family member 11 |
ACAD-11 |
Curated: Coronary artery disease, Developmental and epileptic encephalopathy, Gout
Unreviewed: Renal cell carcinoma
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192
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|
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Acyl-CoA dehydrogenase family member 8 |
ACAD-8, ARC42, IBDH |
Curated: Isobutyryl-coa dehydrogenase deficiency, Obesity, Stomach neoplasms
Unreviewed: 3-hydroxy-3-methylglutaryl-CoA synthase deficiency, Adenoma, Alpha 1-Antitrypsin Deficiency, Alzheimer disease, Anal Canal carcinoma, Anemia, Angioimmunoblastic T-cell lymphoma, Ankylosing Spondylitis, Anxiety Disorder, Appendicitis, Arthritis, Arthropathy, Asthma, Autism, Autoimmune Diseases, Bile duct carcinoma, Breast Cancer, Breast Carcinoma, Capsular cataract, Cardiomyopathy, Celiac disease, Childhood obesity, Cholangiocarcinoma, Cholangitis, Colitis, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal Neoplasms, Crohn Disease, Deficiency Of Butyryl-CoA Dehydrogenase, Dental Diseases, Diabetes Insipidus, Diabetes Mellitus, Diverticulitis, Dysequilibrium Syndrome, Enterocolitis, Enthesitis, Eosinophilia, Erythema nodosum, Fanconi Anemia, Functional Gastrointestinal Disorders, Gastric Cancer, Gastroenteritis, Gastrointestinal Diseases, Glucocorticoid Receptor Deficiency, Gluten intolerance, Granulomatous Disease, Hamartoma, Hemorrhoids, Hidradenitis suppurativa, Ichthyosis Bullosa Of Siemens, immunodeficiency, Immunologic Deficiency Syndromes, Inflammatory Bowel Disease, Intestinal Diseases, Iron deficiency anemia, Irritable Bowel Syndrome, Isobutyryl-CoA Dehydrogenase Deficiency, Kohlschutter syndrome, Kyphoscoliotic Ehlers-Danlos Syndrome, Leprosy, Leukopenia, Lung Cancer, Lung carcinoma, Lymphoproliferative Disorder, Malabsorption Syndrome, Malignant gastrointestinal tract tumors, Malignant Neoplasm, Malnutrition, Mental Depression, Mental Disorders, Metabolic Syndrome, Migraine, Mixed Anxiety And Depressive Disorder, Multiple Sclerosis, Neoplasms, Osteopenia, Osteoporosis, Papilloma, Parkinson disease, Perianal abscess, Polyposis, Portal Vein Thrombosis, Psoriasis, Psoriatic Arthritis, Pulmonary Stenosis, Pyoderma Gangrenosum, Rheumatoid arthritis, Sclerosing Cholangitis, Septicemia, Sexual Dysfunction, Sleep Disorders, Smith-Lemli-Opitz Syndrome, Sphingomyelinase deficiency, Spondyloarthritis, Stomach Neoplasms, Thrombophilia, Thyroiditis, Ulcerative colitis, Uveitis, Vitamin D Deficiency
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193
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|
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Acyl-CoA dehydrogenase family member 9 |
MC1DN20, NPD002 |
Curated: Acyl-coa dehydrogenase 9 deficiency, Mitochondrial complex deficiency
Unreviewed: Acyl CoA Dehydrogenase Deficiency, Cardiomegaly, Cardiomyopathy, Congestive Heart Failure, Developmental disability, Epileptic encephalopathy, Fatty Liver, Hypertrophic cardiomyopathy, Hypoglycemia, Immune system disease, Lactic acidosis, Liver failure, Lymphoma, Mitochondrial Complex Deficiency, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Myasthenia Gravis, Myopathy, Nervous System Disorder, Optic atrophy, Parkinson disease, Stroke, Ventricular hypertrophy
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194
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|
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ACAD9 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
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195
|
|
|
Acyl-CoA dehydrogenase long chain |
ACAD4, LCAD |
Curated: Basal cell carcinoma, Insomnia, Very long chain acyl-coa dehydrogenase deficiency
Unreviewed: Acyl CoA Dehydrogenase Deficiency, Autism, Colorectal neoplasm, Diabetes mellitus, type 2, Esophagus Neoplasm, Expressive language delay, Fatty Liver, Hepatocellular carcinoma, Hypertrophic cardiomyopathy, Hypoglycemia, Kidney Disease, Kidney Failure, Liver Cancer, Lung neoplasms, Malignant Neoplasm, Meningioma, Mitochondrial disease, Myasthenia Gravis, Neoplasms, Osteoarthritis, Sjogren syndrome, Squamous cell carcinoma, Stomach neoplasms
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196
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|
|
Acyl-CoA dehydrogenase medium chain |
ACAD1, MCAD, MCADH |
Curated: Congenital hydrocephalus, Liver failure, Obesity, Infantile spasms, medium chain acyl-coa dehydrogenase deficiency
Unreviewed: Attention deficit hyperactivity disorder, Breast Cancer, Breast Carcinoma, Cerebral palsy, Colorectal Cancer, Congestive Heart Failure, Crisponi syndrome, Developmental Delay, Distal arthrogryposis, Dyslipidemias, Fatty Liver, Febrile seizures, Glioblastoma, Glioma, Glycogen Storage Disease, Heart Failure, Hydrocephalus, Congenital, With Or Without Brain Or Eye Anomalies, Hyperglycinuria, Hypoglycemia, Hypoglycemic coma, Inborn Errors Of Metabolism, Inflammatory bowel disease, Ketosis, Left Ventricular Hypertrophy, Long QT Syndrome, Macrocephaly, Medium Chain Acyl-CoA Dehydrogenase Deficiency, Metabolic Diseases, Metabolic syndrome, Mitochondrial disease, Myopathy, Necrotizing Enterocolitis, Neoplasms, Neuroblastoma, Neurodegenerative Disorders, Osteoporosis, Peritonitis, Phenylketonuria, Psoriatic Arthritis, Renal Carcinoma, Renal Carnitine Transport Defect, Renal cell carcinoma, Seizure, Ulcerative colitis, Very long-chain acyl-coa dehydrogenase deficiency
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197
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|
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Acyl-CoA dehydrogenase short chain |
ACAD3, SCAD |
Curated: Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cannabis abuse, Congestive heart failure, Butyryl-coa dehydrogenase deficiency, Heart failure, Major depressive disorder, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2, short chain acyl-coa dehydrogenase deficiency
Unreviewed: Bipolar Disorder, Cardiomyopathy, Chronic obstructive pulmonary disease, Colorectal neoplasm, Congestive Heart Failure, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Coronary Syndrome, Deficiency Of Butyryl-CoA Dehydrogenase, Developmental Delay, Diabetes mellitus, type 2, Epilepsy, Erythema, Facial paralysis, Heart Failure, Hepatocellular carcinoma, Inflammatory bowel disease, Kidney Disease, Kidney Failure, Liver carcinoma, Lung disease, Malignant Neoplasm, Medium Chain Acyl-CoA Dehydrogenase Deficiency, Myocardial Infarction, Myopathy, Neoplasms, Pancreatic cancer, Pancreatic carcinoma, Prader-Willi Syndrome, Psychosis, Scoliosis, Short Chain Acyl-CoA Dehydrogenase Deficiency
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198
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|
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Acyl-CoA dehydrogenase short/branched chain |
2-MEBCAD, ACAD7, SBCAD |
Curated: 2-methylbutyryl-coa dehydrogenase deficiency, Autism, Lewy body disease, Periodontitis, Rheumatic disease
Unreviewed: 2-methylbutyryl-CoA dehydrogenase deficiency, 3-hydroxy-3-methylglutaryl-CoA synthase deficiency, Amyotrophy, Breast Cancer, Breast Carcinoma, Deficiency Of Butyryl-CoA Dehydrogenase, Developmental Delay, Diabetes Mellitus, Exotropia, Hepatocellular carcinoma, Hyperlipidemia, Hypertension, Hypoglycemia, Isobutyryl-CoA Dehydrogenase Deficiency, Kohlschutter syndrome, Kyphoscoliotic Ehlers-Danlos Syndrome, Liver carcinoma, Liver neoplasm, Microcephaly, Motor delay, Renal cell carcinoma, Smith-Lemli-Opitz Syndrome
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199
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|
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Acyl-CoA dehydrogenase very long chain |
ACAD6, LCACD, VLCAD |
Curated: Autism, Cardiac arrhythmia, Dilated cardiomyopathy, Cardiomyopathy, Hearing loss, Hypoxia, Intellectual developmental disorder, Myopathy, Very long chain acyl-coa dehydrogenase deficiency, Yorifuji okuno syndrome
Unreviewed: Acyl CoA Dehydrogenase Deficiency, Adrenocortical adenoma, Adrenogenital Syndrome, Agenesis Of Corpus Callosum, Alpha 1-Antitrypsin Deficiency, Aplasia Cutis Congenita, Atrioventricular block, Complement Component Deficiency, Congenital abnormalities, Congenital adrenal hyperplasia, Dermatitis, Fatty Liver, Hearing Loss, Heart failure, Hepatocellular carcinoma, Hypertrophic cardiomyopathy, Hypoglycemia, Hypoproteinemia, Idiopathic pulmonary fibrosis, Leukemia, Macrocephaly, Metabolic Myopathy, Mitochondrial trifunctional protein deficiency, Myeloid leukemia, Obesity, Osteosarcoma, Patent foramen ovale, Pearson`s Marrow-Pancreas Syndrome, Pericardial effusion, Respiratory Failure, Rhabdomyolysis, Sjogren syndrome, Trifunctional protein deficiency, Ventricular Fibrillation, Ventricular septal defect, Ventricular tachycardia, Very long-chain acyl-coa dehydrogenase deficiency, Von Willebrand Disorder
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200
|
|
|
Aggrecan |
AGC1, AGCAN, CSPG1, CSPGCP, MSK16, SEDK, SSOAOD |
Curated: Short stature spectrum, Aortic stenosis, Aortic valve disease, Rheumatoid arthritis, Color vision deficiency, Desbuquois syndrome, Dupuytren contracture, Hearing loss, Meniere disease, Obesity, Osteoarthritis, Spondyloepimetaphyseal dysplasia, Spondyloepiphyseal dysplasia
Unreviewed: Achondroplasia, Alzheimer disease, Amyloidosis, Anaplasia, Angiofibroma, Aortic disease, Aortic dissection, Aortic Valve Disease, Arteriosclerosis, Arthritis, Arthropathy, Asthma, Atherosclerosis, Autism, Autism Spectrum Disorder, Autoimmune Diseases, Bicuspid aortic valve, Bone Disease, Bone marrow diseases, Brachydactyly, Breast neoplasm, Bronchospasm, Cardiovascular Diseases, Carpal Tunnel Syndrome, Cartilage disease, Cerebral hypomyelination, Chondroblastoma, Chondrodysplasia, Chondromalacia, Chondrosarcoma, Chordoma, Colonic Neoplasms, Congenital abnormalities, Developmental disability, Developmental dysplasia of the hip, Diabetes Mellitus, Dowling-Degos Disease, Dwarfism, Dysmorphic Features, Endometrial neoplasm, Facial dysmorphism syndrome, Facioscapulohumeral Muscular Dystrophy, Frontal bossing, Graves ophthalmopathy, Growth disorder, Head and neck neoplasm, Hemochromatosis, Hypogonadotropic Hypogonadism, Hypoplasia Of Thumb, Hypoxia, Infective arthritis, Interstitial cystitis, Intervertebral Disc Degeneration, Intervertebral disc disease, Intervertebral Disc Disorder, Intervertebral disc displacement, Juvenile arthritis, Kashin-Beck Disease, Kidney disease, Knee osteoarthritis, Laryngeal carcinoma, Laryngeal neoplasm, Leiomyoma, Lhermitte-Duclos disease, Lipoma, Lipomatosis, Liposarcoma, Liver carcinoma, Lumbar Disc Disease, Macrocephaly, Malocclusion, Mesomelia, Metabolic syndrome, Micromelia, Mitral valve prolapse, Mucopolysaccharidosis, Multiple Congenital Anomalies, Multiple congenital exostosis, Multiple Epiphyseal Dysplasia, Multiple myeloma, myofibromatosis, Myopia, Neoplasms, Obsessive-Compulsive Disorder, Orofacial cleft, Osteoarthritis Of Hip, Osteochondritis Dissecans, Osteochondrodysplasia, Osteochondrodysplasias, Osteoporosis, Otosclerosis, Periodontitis, Pituitary dwarfism, Polyarthritis, Polycystic Ovary Syndrome, Premature osteoarthritis, Progeria, Prune belly syndrome, Pseudoachondroplasia, Rhizomelia, Sacroiliitis, Salivary gland disease, Sarcoma, Schizophrenia, Scoliosis, Short Stature-Advanced Bone Age Osteoarthritis Syndrome, Skeletal Dysplasia, Slipped Capital Femoral Epiphyses, Spondyloepiphyseal dysplasia congenita, Stomach neoplasms, Tendinopathy, Uveitis, Varicose veins, Williams syndrome
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