2751
|
|
|
Centlein |
C9orf101, C9orf39, bA340N12.1 |
|
2752
|
|
|
Contactin 1 |
CMYO12, CMYP12, F3, GP135, MYPCN |
Alzheimer disease, Astrocytoma, Bipolar disorder, Central nervous system cancer, Compton-north congenital myopathy, Congenital lethal myopathy , Congenital myopathy, Dementia, Dry eye syndrome, Glioma, Major depressive disorder, Parkinson disease, Schizophrenia, Spondylosis |
2753
|
|
|
Contactin 2 |
AXT, EPEO5, FAME5, TAG-1, TAX, TAX1 |
Benign myoclonic epilepsy, Neurodevelopmental disorder, Diabetes mellitus, Early onset epilepsy with developmental delay, Familial adult myoclonic epilepsy, Adult myoclonic epilepsy, Gout, Non-specific syndromic intellectual disability, Periodontitis, Schizophrenia, Diabetes mellitus type 2 |
2754
|
|
|
Contactin 3 |
BIG-1, PANG, PCS |
|
2755
|
|
|
Contactin 4 |
AXCAM, BIG-2 |
Amyotrophic lateral sclerosis, Anorexia nervosa, Attention deficit hyperactivity disorder, Atypical femoral fracture, Autism, B-cell acute lymphoblastic leukemia, Bipolar disorder, Neurodevelopmental disorder, Craniofacial abnormalities, Developmental disability, Gallbladder neoplasms, Growth disorder, Major depressive disorder, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder, Oropharyngeal cancer, Psoriasis, Psoriatic arthritis, Schizophrenia, Scoliosis, Thoracic aortic aneurysm, Tourette syndromeView all (7 more) |
2756
|
|
|
Contactin 5 |
HNB-2s, NB-2 |
Anxiety disorder, Astrocytoma, Atrial fibrillation, Basal cell carcinoma, Behcet disease, Bipolar disorder, Central nervous system cancer, Obstructive pulmonary disease, Circadian rhythm sleep disorder, Liver cirrhosis, Color vision deficiency, Colorectal cancer, Crohn disease, Dementia, Diabetic ketoacidosis, Digestive system disease, Glioblastoma, Glioma, Gout, Hyperuricemia, Insomnia, Large artery stroke, Major depressive disorder, Multiple sclerosis, Neurotic disorder, Nonalcoholic fatty liver disease, Obesity, Pernicious anemia, Psychiatric disorders, Schizophrenia, Scoliosis, Splenic disease, Diabetes mellitus type 1, Venous thromboembolismView all (19 more) |
2757
|
|
|
Contactin 6 |
NB3 |
Autism, Bipolar disorder, Adenoid cystic carcinoma, Color vision deficiency, Neurodevelopmental disorder, Cutaneous mastocytosis, Tourette syndrome, Non-specific syndromic intellectual disability, Ocular hypotension, Oligodendroglioma, Prostate cancer, Schizophrenia, Systemic lupus erythematosus |
2758
|
|
|
Contactin associated protein 1 |
CASPR, CHN3, CNTNAP, NRXN4, P190 |
Arthrogryposis multiplex congenita, Distal arthrogryposis, Breast cancer, Charcot-marie-tooth disease, Congenital deformity of clavicle, Congenital deformity of elbow, Congenital deformity of forearm, Congenital deformity of scapula, Congenital deformity of wrist, Congenital dislocation of elbow, Congenital glenohumeral joint dislocation, Lethal congenital contracture syndrome, Major depressive disorder, Neuropathy, congenital hypomyelinating, Pena-shokeir syndrome |
2759
|
|
|
Contactin associated protein 2 |
AUTS15, CASPR2, CDFE, NRXN4, PTHSL1 |
Alzheimer disease, Asthma, Autism, Bipolar disorder, Breast cancer, Cataract, Charcot-marie-tooth disease, Developmental and epileptic encephalopathy, Colorectal cancer, Colonic neoplasms, Neurodevelopmental disorder, Cortical dysplasia-focal epilepsy syndrome, Crohn disease, Dementia, Diabetic neuropathy, Epilepsy, Rolandic epilepsy, Gastroesophageal reflux disease, Glaucoma, Gout, Hyperkinesia, Idiopathic pulmonary fibrosis, Inflammatory bowel disease, Intellectual developmental disorder, Irritable bowel syndrome, Language development disorders, Major depressive disorder, Metabolic syndrome, Nonalcoholic fatty liver disease, Non-specific syndromic intellectual disability, Obesity, Oligodendroglioma, Parkinson disease, Peptic ulcer disease, Prostate cancer, Psychiatric disorders, Willis-ekbom disease, Schizophrenia, Scoliosis, Small cell lung carcinoma, Specific language disorder, Diabetes mellitus type 2, Ulcerative colitis, Depression, Vascular dementiaView all (30 more) |
2760
|
|
|
Contactin associated protein family member 4 |
CASPR4 |
|
