|
991
|
|
|
Carbonic anhydrase 2 |
CA-II, CAC, CAII, Car2, HEL-76, HEL-S-282 |
Autism, Autoimmune pancreatitis, Osteopetrosis, Biliary cirrhosis, Hepatocellular carcinoma, Cholangitis, Desbuquois syndrome, Esophageal squamous cell carcinoma, Systemic lupus erythematosus, Osteoporosis, Pancreatitis, Biliary cholangitis, Rheumatoid arthritis, Sjogren syndrome, Stomach neoplasms |
|
992
|
|
|
Carbonic anhydrase 3 |
CAIII, Car3 |
|
|
993
|
|
|
Carbonic anhydrase 4 |
CAIV, Car4, RP17 |
|
|
994
|
|
|
Carbonic anhydrase 5A |
CA5, CA5AD, CAV, CAVA, GS1-21A4.1 |
|
|
995
|
|
|
Carbonic anhydrase 8 |
CA-RP, CA-VIII, CALS, CAMRQ3, CARP, SCAR34 |
Cerebellar ataxia, Cerebellar ataxia, intellectual disability, and dysequilibrium, Cerebellar ataxia, mental retardation, and dysequilibrium, Dysequilibrium syndrome, Intellectual developmental disorder, Obesity, Parkinson disease, Spinocerebellar ataxia |
|
996
|
|
|
Carbonic anhydrase 9 |
CAIX, MN |
|
|
997
|
|
|
Carbonic anhydrase 12 |
CA-XII, CAXII, HsT18816, T18816 |
|
|
998
|
|
|
Calcium voltage-gated channel subunit alpha1 A |
APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2, EIEE42, FHM, HPCA, MHP, MHP1, SCA6 |
Alzheimer disease, Amyotrophic lateral sclerosis, Ataxia, Spinocerebellar ataxia, Auditory neuropathy, Bipolar disorder, Bulbar palsy, Cannabis abuse, Cerebellar ataxia, Cerebellar atrophy, Cerebral palsy, Chorea, Kidney disease, Color vision deficiency, Congenital neurologic anomalies , Vascular dementia, Developmental and epileptic encephalopathy, Dysarthria, Endometriosis, Absence epilepsy, Generalized epilepsy, Episodic ataxia, Gastroesophageal reflux disease, Global developmental delay, Gross motor development delay, Hemiplegic migraine, Intellectual developmental disorder, Lennox-gastaut syndrome, Major depressive disorder, Migraine, Neurodevelopmental disorder, Neurodevelopmental disorders, Non-small cell lung carcinoma, Spastic ataxia, Strabismus, Substance abuseView all (21 more) |
|
999
|
|
|
Calcium voltage-gated channel subunit alpha1 B |
BIII, CACNL1A5, CACNN, Cav2.2, DYT23, NEDNEH |
|
|
1000
|
|
|
Calcium voltage-gated channel subunit alpha1 C |
CACH2, CACN2, CACNA1C-IT2, CACNL1A1, CCHL1A1, CaV1.2, LQT8, NEDHLSS, TS, TS. LQT8 |
Anhedonia, Anorexia nervosa, Anxiety disorder, Cardiac arrhythmias, Attention deficit hyperactivity disorder, Atypical femoral fracture, Timothy syndrome, Autism, Bipolar disorder, Brugada syndrome, Cardiac arrhythmia, Cardiomyopathy, Cerebral palsy, Cognition disorder, Color vision deficiency, Bipolar depression, Major depressive disorder, Epilepsy, Esophageal atresia, Long qt syndrome, Genetic predisposition to disease, Glomerulonephritis, Gout, Hepatitis b, Hypertension, Hypertrophic cardiomyopathy, Hypoglycemia, Inflammatory bowel disease, Intellectual developmental disorder, Congenital anomaly of limb, Depression, Metabolic syndrome, Mood disorder, Neurodevelopmental disorder, Neurodevelopmental disorders, Non-organic psychosis, Non-specific syndromic intellectual disability, Obesity, Obsessive-compulsive disorder, Oligodendroglioma, Pancreatic cancer, Polymorphic catecholaminergic ventricular tachycardia, Psychiatric disorders, Psychotic disorders, Restrictive cardiomyopathy, Schizophrenia, Scoliosis, Short qt syndrome, Tourette syndrome, Diabetes mellitus, type 2, Ulcerative colitis, Ventricular fibrillation, Wolff-parkinson-white syndromeView all (38 more) |
