|
1291
|
|
|
Carbohydrate sulfotransferase 3 |
C6ST, C6ST1, HSD |
Cubitus valgus, Acquired kyphoscoliosis, Aortic valve insufficiency, Aortic valve sclerosis, Arthropathy, Bicuspid aortic valve, Brachycephaly, Brachydactyly, Chondrodystrophic myotonia, Talipes equinovalgus, Congenital clubfoot, Congenital kyphoscoliosis, Cutis laxa, Developmental delay, Dwarfism, Dyschondroplasias, Elbow flexion contracture, Esotropia, Frontal bossing, Glaucoma, Glaucoma, congenital, High palate, Hydrocephalus, Hyperopia, Larsen syndrome, Left ventricular hypertrophy, Melnick-needles syndrome, Microdontia, Microstomia, Microtia, Mitral valve prolapse, Mitral valve stenosis, Motor delay, Multiple epiphyseal dysplasia, Osteochondrodysplasia, Osteopenia, Osteoporosis, Patent foramen ovale, Pulmonary arterial hypertension, Pulmonary stenosis, Radioulnar synostosis, Rhizomelia, Schwartz-jampel syndrome, Scoliosis, Skeletal dysplasia, Spondyloenchondrodysplasia, Spondyloepiphyseal dysplasia congenita, Spondyloepiphyseal dysplasia, Tricuspid valve insufficiency, Tricuspid valve stenosis, Van buchem disease, Ventricular hypertrophy, Ventricular septal defectView all (38 more) |
|
1292
|
|
|
CD34 molecule |
- |
|
|
1293
|
|
|
CD36 molecule (CD36 blood group) |
BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV, PASIV, SCARB3 |
Antibody deficiency syndrome, Cardiomyopathy, Celiac disease, Coronary heart disease, Dermatitis, Hypertension, Immunologic deficiency syndromes, Impaired cognition, Kidney disease, Myocardial ischemia, Platelet glycoprotein iv deficiency, Platelet-type bleeding disorder |
|
1294
|
|
|
CD38 molecule |
ADPRC 1, ADPRC1, cADPR1 |
|
|
1295
|
|
|
C-X-C motif chemokine ligand 14 |
BMAC, BRAK, KEC, KS1, MIP-2g, MIP2G, NJAC, SCYB14 |
|
|
1296
|
|
|
Chromodomain helicase DNA binding protein 1 like |
ALC1, CHDL |
|
|
1297
|
|
|
Centrosomal protein 41 |
JBTS15, TSGA14 |
Agenesis of corpus callosum, Autism spectrum disorder, Cerebellar vermis agenesis, Ciliopathies, Congenital cerebral hernia, Congenital coloboma of iris, Developmental delay, Dextrocardia, Disorder of eye, Fundus coloboma, Hirschsprung disease, Hydrocephalus, Joubert syndrome, Joubert syndrome with ocular defect, Joubert syndrome, digenic, Mental retardation, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Oral cleft, Penis agenesis, Polydactyly, Polydactyly of toes, Polymicrogyria, Ptosis, Retinal coloboma, Retinal dystrophy, Schizophrenia, Scoliosis, Situs inversus, StrabismusView all (16 more) |
|
1298
|
|
|
Clock circadian regulator |
KAT13D, bHLHe8 |
|
|
1299
|
|
|
CDC42 binding protein kinase beta |
CHOCNS, MRCKB |
|
|
1300
|
|
|
CD40 molecule |
Bp50, CDW40, TNFRSF5, p50 |
Ankylosing spondylitis, Autoimmune diseases, Breast cancer, Mammary neoplasms, Breast carcinoma, Cholangitis, Compensatory hyperinsulinemia, Crohn disease, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Grand mal status epilepticus, Hyper-igm immunodeficiency syndrome, Hyper-igm syndrome, Hyperglycemia, Hyperimmunoglobulin m syndrome, Hyperinsulinism, Immune system diseases, Immunologic deficiency syndromes, Kawasaki disease, Lupus erythematosus, Marfan syndrome, Multiple sclerosis, Neutropenia, Nonconvulsive status epilepticus, Obesity, Petit mal status, Psoriasis, Rheumatoid arthritis, Status epilepticus, Ulcerative colitisView all (15 more) |
