|
191
|
|
|
Carbohydrate sulfotransferase 14 |
ATCS, D4ST1, EDSMC1, HNK1ST |
Adducted thumbs syndrome, Arachnodactyly, Arthrogryposis multiplex congenita, Atrial septal defect, Brachycephaly, Congenital clubfoot, Congenital exomphalos, Congenital malrotation of intestine, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Distal arthrogryposis, Musculocontractural ehlers-danlos syndrome, Glaucoma, Hiatal hernia, High palate, Hydronephrosis, Microcornea, Microstomia, Motor delay, Mouth abnormalities, Myopia, Hypotonia, Nephrotic syndrome, Posteriorly rotated ear, Prostatic neoplasms, Prostate cancer, Retinal detachment, Scoliosis, StrabismusView all (15 more) |
|
192
|
|
|
Cholinergic receptor muscarinic 4 |
HM4, M4R |
|
|
193
|
|
|
Chromosome 12 open reading frame 57 |
C10, GRCC10 |
Agenesis of corpus callosum, Aortic aneurysm, Aortic valve insufficiency, Atrophy of kidney, Attention deficit hyperactivity disorder, Brachydactyly, Camptodactyly of fingers, Congenital clubfoot, Congenital coloboma of iris, Developmental delay, Dolichocephaly, Epilepsy, Frontal bossing, Fundus coloboma, Hydronephrosis, Hypoplasia of teeth, Mental retardation, Macrocephaly, Micrognathism, Microphthalmos, Microphthalmos co-occurrent with congenital ocular coloboma, Myopia, Retinal coloboma, Temtamy syndrome, Vesicoureteral refluxView all (10 more) |
|
194
|
|
|
Cholinergic receptor muscarinic 5 |
HM5 |
|
|
195
|
|
|
Chymotrypsin C |
CLCR, ELA4 |
Anorexia, Biliary hyperplasia, Choledochal cyst, Cholesterol gallstones, Diabetes mellitus, Exocrine pancreatic insufficiency, Hereditary pancreatitis, Leukemia, Lupus erythematosus, Lymphoma, Pancreas divisum, Pancreatic pseudocyst, Pancreatitis, Pleural effusion, Sphincter of oddi dyskinesia, Splanchnic vein thrombosis, Tropical calcific pancreatitis, Tropical pancreatitisView all (3 more) |
|
196
|
|
|
Cholinergic receptor nicotinic alpha 1 subunit |
ACHRA, ACHRD, CHRNA, CMS1A, CMS1B, CMS2A, FCCMS, SCCMS |
Akinesia, Aplasia of muscle, Arthrogryposis multiplex congenita, Autism, Bulbar palsy, Cirrhosis, Congenital epicanthus, Myasthenic syndrome, Pulmonary hypoplasia, Developmental delay, Dysarthria, Dysphagia, Facial paralysis, High palate, Hydrops fetalis, Lethal multiple pterygium syndrome, Leukemia, Cystic hygroma, Macrotia, Micrognathism, Motor delay, Multiple pterygium syndrome, Myasthenia gravis, Hypotonia, Pena shokeir syndrome, Ptosis, Respiratory failure, ScoliosisView all (13 more) |
|
197
|
|
|
Cholinergic receptor nicotinic alpha 2 subunit |
- |
|
|
198
|
|
|
Cholinergic receptor nicotinic alpha 3 subunit |
BAIPRCK, LNCR2, NACHRA3, PAOD2 |
Chronic obstructive pulmonary disease, Clonic seizures, Congenital anomalies of kidney and urinary tract, Coronary heart disease, Development disorder, Dysautonomia, Bronchitis, Hypotonic seizures, Jacksonian seizure, Lung neoplasms, Lung carcinoma, Lung adenocarcinoma, Lung cancer, Nasopharyngeal carcinoma, Schizophrenia, SeizureView all (1 more) |
|
199
|
|
|
Cytochrome P450 family 2 subfamily U member 1 |
P450TEC, SPG49, SPG56 |
|
|
200
|
|
|
Cholinergic receptor nicotinic alpha 4 subunit |
BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 |
Acth deficiency, Attention deficit hyperactivity disorder, Autism, Clonic seizures, Development disorder, Epilepsy, Hypotonic seizures, Jacksonian seizure, Mental depression, Minimal brain dysfunction, Nervous system disorder, Nocturnal epilepsy, Schizophrenia, Seizure, Short sleeper syndromes, Sleep disorders, Sleep wake disordersView all (2 more) |
