2471
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Coenzyme A synthase |
DPCK, NBIA6, NBP, PCH12, PPAT, UKR1, pOV-2 |
Curated: Coasy protein-associated neurodegeneration, Coenzyme a synthase protein associated neurodegeneration, Hallervorden spatz syndrome, Metabolic syndrome, Mucopolysaccharidosis, Neurodegeneration with brain iron accumulation, Pontocerebellar hypoplasia, Diabetes mellitus type 2
Unreviewed: Achromatopsia, Adrenal hyperplasia, Adrenocortical adenoma, Alzheimer disease, Amyotrophic lateral sclerosis, Arthrogryposis, Arthrogryposis multiplex congenita, Bone Disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cerebellar Hypoplasia, Cerebral Infarction, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Ciliary Dyskinesia, COASY Protein-Associated Neurodegeneration, Coenzyme A Synthase Protein Associated Neurodegeneration, Cognition disorder, Cognitive disorder, Colorectal Cancer, Colorectal neoplasm, Congenital adrenal hyperplasia, Cushing`s Syndrome, Cystic Fibrosis, Dementia, Developmental Delay, Developmental regression, Diabetes Mellitus, Diabetic foot, Distal amyotrophy, Dwarfism, Dysarthria, Dyschromatosis Universalis Hereditaria, Dysmyelinating Leukodystrophy And Spastic Paraparesis With Or Without Dystonia, Endometrial carcinoma, Fatty Acid Hydroxylase Associated Neurodegeneration, Fibrous dysplasia, Head and neck cancer, Head And Neck Carcinoma, Hepatocellular carcinoma, Hyperphosphatemia, Hypertension, Hypoparathyroidism, Hypoplasia Of Corpus Callosum, Hypothyroidism, Impaired Cognition, Ischemic Stroke, Lateral Sclerosis, Leukemia, Leydig Cell Tumor, Limb-Girdle Muscular Dystrophy, Liver carcinoma, Liver neoplasms, Malignant Neoplasm, McCune-Albright Syndrome, Melanoma, Mental Depression, Microcephaly, Micrognathism, Myocardial Ischemia, Neoplasms, Nephropathy with Pretibial Epidermolysis Bullosa and Deafness, Neuroblastoma, Neurodegeneration With Brain Iron Accumulation, Neurodegenerative disorder, Non-Alcoholic Fatty Liver Disease, Obesity, Obsessive-Compulsive Disorder, Osteogenesis Imperfecta, Osteoporosis, Ovarian cancer, Ovarian Carcinoma, Ovarian Cysts, Ovarian Epithelial carcinoma, Pancreatic adenocarcinoma, Pancreatic Cyst, Parkinson disease, Peripheral axonal neuropathy, Polyostotic Fibrous Dysplasia, Pontoneocerebellar hypoplasia, Precocious puberty, Prostatic neoplasm, Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism, Rectal Carcinoma, Renal cell carcinoma, Somatotroph Adenoma, Spastic Quadriplegia, Stomach Carcinoma, Stomach Neoplasms, Stroke, Thyroid Gland Follicular Adenoma, Triple negative breast cancer, Uveal Melanoma, Vitamin D Deficiency, Xeroderma pigmentosum
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2472
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Cordon-bleu WH2 repeat protein |
- |
Curated: Autoimmune disease, Central nervous system cancer, Chromosomal disorder, Glioblastoma, Glioma, Major depressive disorder, Nasal disorder, Oligodendroglioma, Osteoarthritis, Squamous cell carcinoma, Diabetes mellitus type 1, Diabetes mellitus type 2, Vascular disease
Unreviewed: Alzheimer disease, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Leukemia, Lung carcinoma, Lymphoblastic Leukemia, Lymphocytic Leukemia, Metabolic syndrome, Obesity
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2473
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Cordon-bleu WH2 repeat protein like 1 |
COBLR1 |
Curated: Cleft lip and palate, Coronary artery disease, Diabetes mellitus, Diabetic eye disease, Diabetic neuropathy, Diabetic retinopathy, Hyperlipidemia, Gout, Metabolic syndrome, Myocardial ischemia, Nonalcoholic fatty liver disease, Psoriasis, Diabetes mellitus type 2, Diabetic nephropathy type 2, Uterine fibroid
Unreviewed: Autism, Autism Spectrum Disorder, Blast crisis, Blast phase chronic myelogenous leukemia, Carcinogenesis, Cleft lip, Cleft palate, Diabetes Mellitus, Diabetes mellitus, type 2, Gestational diabetes, Mesothelioma, Myeloid Leukemia, Obesity, Prostate cancer, Renal cell carcinoma, Tourette Syndrome
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2474
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COBL pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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2475
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Cochlin |
COCH-5B2, COCH5B2, DFNA9, DFNB110 |
Curated: Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital hearing disorder, Deafness, Esophageal adenocarcinoma, Hearing loss, Hereditary hearing loss, Hypertension, Nephrotic syndrome, Usher syndrome, nonsyndromic genetic hearing loss
Unreviewed: Atrophy, Bilateral Vestibulopathy, Cognition disorder, DYSTROPHIC EPIDERMOLYSIS BULLOSA, Glaucoma, Headache, Hearing Loss, Impaired Cognition, Low-frequency hearing loss, Memory disorders, Meniere Disease, Neurodegenerative Disorders, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Nyctalopia, Osteoporosis, Sensorineural hearing loss, Triple negative breast cancer, Usher Syndrome, Vestibular disease, Vestibular Diseases, von Willebrand disorder
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2476
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COCH antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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2477
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- |
CORDX2 |
Curated: N/A
Unreviewed: N/A
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2478
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Component of oligomeric golgi complex 1 |
CDG2G, LDLB |
Curated: Congenital disorder of glycosylation, Desbuquois syndrome, Nephrotic syndrome, COG1-congenital disorder of glycosylation
Unreviewed: Abnormal spinal segmentation, Acquired Kyphoscoliosis, Anemia, Burkitt`s Lymphoma, Cerebellar atrophy, Cerebral Atrophy, Cerebrocostomandibular Syndrome, Cerebrocostomandibular-Like Syndrome, Congenital Camptodactyly, Congenital Clubfoot, Congenital kyphoscoliosis, Cryptorchidism, Developmental Delay, Esophageal squamous cell carcinoma, Hematologic Neoplasms, High palate, Hydronephrosis, Hypospadias, Lymphocytic Leukemia, Mental retardation, Micrognathism, Microstomia, Microtia, Nervous system disease, Osteopenia, Pierre-Robin Syndrome, Pulmonary arterial hypertension, Renal cell carcinoma, Renal Insufficiency, Rhizomelia, Rib fusion, Scoliosis, Temporal cortical atrophy
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2479
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Component of oligomeric golgi complex 2 |
CDG2Q, LDLC |
Curated: Congenital disorder of glycosylation, Ulcerative colitis, congenital disorder of glycosylation, type IIq
Unreviewed: Amyotrophic lateral sclerosis, Atrial Fibrillation, Cardiovascular disease, Cardiovascular Diseases, Cerebral microangiopathy, Coronary artery disease, Dementia, Developmental Delay, Diabetes Mellitus, Diabetes mellitus, type 1, Dyslipidemias, Fatty liver, Hypercholesterolemia, Hyperlipoproteinemia, Hypoalphalipoproteinemia, Hypoplasia Of Corpus Callosum, Iga nephropathy, Myocardial infarction, Myotonic dystrophy, Obesity, Rheumatoid arthritis, Sitosterolemia, Spastic Quadriplegia, Stomach Carcinoma, Stomach Neoplasms
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2480
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Component of oligomeric golgi complex 3 |
CDG2BB, SEC34 |
Curated: Congenital disorder of glycosylation
Unreviewed: Breast Cancer, Developmental disability, Epilepsy, Facial dysmorphism syndrome, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Microcephaly, Myeloid leukemia, Neoplasms, Renal cell carcinoma
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