5551
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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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5552
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COBL pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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5553
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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, Deafness, autosomal dominant 9, Deafness, autosomal recessive 110
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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5554
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COCH antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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5555
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- |
CORDX2 |
Curated: N/A
Unreviewed: N/A
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5556
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Component of oligomeric golgi complex 1 |
CDG2G, LDLB |
Curated: Congenital disorder of glycosylation, Desbuquois syndrome, Nephrotic syndrome
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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5557
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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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5558
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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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5559
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Component of oligomeric golgi complex 4 |
CDG2J, COD1, SWILS |
Curated: Congenital disorder of glycosylation, Desbuquois syndrome, Gross motor development delay, Metabolic syndrome, Saul-wilson syndrome, Diabetes mellitus type 2, Microcephalic osteodysplastic dysplasia, Saul-Wilson type
Unreviewed: Apraxia, Blood Coagulation Disorders, Cataract, Cerebral Atrophy, Cirrhosis, Cone Dystrophy, Congenital bilateral ptosis, Congenital Clubfoot, Congenital Pectus Carinatum, Congenital Pectus Excavatum, Developmental Delay, Diabetic neuropathy, Dwarfism, Epiphyseal dysplasia, Frontal bossing, Frontotemporal cerebral atrophy, Hearing Loss, Hepatolenticular degeneration, Hypercholesterolemia, Hypoplasia Of Corpus Callosum, Isolated Somatotropin Deficiency, Macrocephaly, Microcephalic osteodysplastic dysplasia, Microcephaly, Micrognathism, Motor delay, Nervous system disease, Neutropenia, Nyctalopia, Nystagmus, Proptosis, Renal cell carcinoma, Retinitis Pigmentosa, Seizure, Sensorineural hearing loss
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5560
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Component of oligomeric golgi complex 5 |
CDG2I, GOLTC1, GTC90 |
Curated: Atrial fibrillation, Congenital disorder of glycosylation, Coronary artery disease, Dyslexia, Insomnia, Osteoarthritis, Congenital disorder of glycosylation type iii
Unreviewed: Arthritis, Ataxia with vitamin e deficiency, Atrial Fibrillation, Autism, Brainstem Atrophy, Central Visual Impairment, Cerebellar atrophy, Cerebellar diseases, Clinodactyly, Cognitive disorder, Cryptorchidism, Dwarfism, Dysmorphic Features, Epiphyseal dysplasia, Friedreich Ataxia, Hearing Loss, High palate, Language development disorders, Leber congenital amaurosis, Mental retardation, Microcephaly, Motor delay, Neurogenic Urinary Bladder, Paroxysmal atrial fibrillation, Penis Agenesis, Posteriorly Rotated Ear, Psychiatric disorders, Retinal degeneration, Strabismus, Uterine Fibroids
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