|
991
|
|
|
Carbonic anhydrase 2 |
CA-II, CAC, CAII, Car2, HEL-76, HEL-S-282 |
Adenocarcinoma, Anemia, Autism spectrum disorder, Carcinoma, Developmental delay, Diaphyseal dysplasia, Distal renal tubular acidosis, Dwarfism, Esophagus neoplasm, Gastric cancer, Liver carcinoma, Malocclusion, Mental retardation, Nervous system diseases, Optic atrophy, Osteopetrosis, Osteopetrosis with renal tubular acidosis, Osteoporosis, Periodic hypokalemic paresis, Renal tubular acidosis, Stomach neoplasmsView all (6 more) |
|
992
|
|
|
Carbonic anhydrase 3 |
CAIII, Car3 |
|
|
993
|
|
|
Carbonic anhydrase 4 |
CAIV, Car4, RP17 |
Cataract, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophyView all (1 more) |
|
994
|
|
|
Carbonic anhydrase 5A |
CA5, CA5AD, CAV, CAVA, GS1-21A4.1 |
|
|
995
|
|
|
Carbonic anhydrase 8 |
CA-RP, CA-VIII, CALS, CAMRQ3, CARP, SCAR34 |
Cataract, Cerebellar ataxia, Cerebellar ataxia, mental retardation, and dysequilibrium syndrome, Cerebellar atrophy, Cerebral palsy, Developmental delay, Dwarfism, Dysarthria, Dysequilibrium syndrome, Mental retardation, Parkinson disease, Strabismus |
|
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 |
Absence seizure, Akinetic petit mal, Alternating hemiplegia, Anxiety disorder, Spinocerebellar ataxia, Attention deficit hyperactivity disorder, Autism, Benign paroxysmal torticollis, Bipolar disorder, Blepharospasm, Bulbar palsy, Cerebellar ataxia, Cerebellar atrophy, Cerebellar hypoplasia, Cerebral atrophy, Developmental delay, Developmental regression, Dwarfism, Dysarthria, Dyscalculia, Dyskinetic syndrome, Dysmorphic features, Dysphagia, Dysphasia, Endometriosis, Epilepsy, Epilepsy and migraine, Epileptic encephalopathy, Episodic ataxia, Esotropia, Exfoliation syndrome, Febrile seizures, Gastroesophageal reflux disease, Hearing loss, Hemiplegia/hemiparesis, Hemiplegic migraine, Hypercholesterolemia, Hyperopia, Hypodontia, Mental depression, Mental retardation, Microcephaly, Migraine, Migraine with aura, Migraine, sporadic hemiplegic, Movement disorders, Multiple congenital anomalies, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Paroxysmal ataxia, Psychosis, Ptosis, Retinitis pigmentosa, Rubral tremor, Seizure, Sensory neuropathy, Sleep apnea, Status epilepticus, Strabismus, Vertical nystagmusView all (46 more) |
|
999
|
|
|
Calcium voltage-gated channel subunit alpha1 B |
BIII, CACNL1A5, CACNN, Cav2.2, DYT23, NEDNEH |
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Central visual impairment, Cerebral atrophy, Choreoathetosis, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Leukemia, Mental retardation, Microcephaly, Movement disorders, Nervous system diseases, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Ptosis, Schizophrenia, Status epilepticus, StrabismusView all (10 more) |
|
1000
|
|
|
Calcium voltage-gated channel subunit alpha1 C |
CACH2, CACN2, CACNA1C-IT2, CACNL1A1, CCHL1A1, CaV1.2, LQT8, NEDHLSS, TS, TS. LQT8 |
Anemia, Anhedonia, Antibody deficiency syndrome, Anxiety disorder, Atrial fibrillation, Atrioventricular block, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Brugada syndrome, Bundle branch block, Cardiomyopathy, Choreoathetosis, Cognitive disorder, Common variable immunodeficiency, Congenital anomaly of limb, Depressed bipolar disorder, Development disorder, Developmental delay, Dysphagia, High palate, Hypertension, Hypertrophic cardiomyopathy, Hypoglycemia, Immunologic deficiency syndromes, Impaired cognition, Infantile spasms, Involutional depression, Involutional paraphrenia, Long qt syndrome, Manic disorder, Mental disorders, Mental depression, Microdontia, Mood disorder, Nonorganic psychosis, Optic atrophy, Paroxysmal ventricular fibrillation, Paroxysmal ventricular tachycardia, Psychosis, Reactive hypoglycemia, Renal carnitine transport defect, Romano-ward syndrome, Salaam seizures, Schizophrenia, Scoliosis, Seizure, Sick sinus syndrome, Stress disorder, Supraventricular tachycardia, Syndactyly, Timothy syndrome, Trifascicular block, Ventricular arrhythmia, Ventricular fibrillationView all (40 more) |
