|
831
|
|
|
Centrosomal protein 55 |
C10orf3, CT111, MARCH, URCC6 |
Anencephaly, Arthrogryposis multiplex congenita, Camptodactyly of fingers, Cataract, Cerebellar hypoplasia, Asplenia, Congenital cerebral hernia, Congenital clubfoot, Congenital hepatic fibrosis, Pulmonary hypoplasia, Cryptorchidism, Cystic liver disease, Dandy-walker syndrome, Double ureter, Fibrosis of pancreas, Foot polydactyly, Hydranencephaly, Hydranencephaly with renal aplasia-dysplasia, Hydrocephalus, Liver carcinoma, Lobar holoprosencephaly, Cystic hygroma, Male pseudohermaphroditism, Meckel syndrome, Meckel-gruber syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Optic atrophy, Sclerocystic ovaries, Pancreatic cyst, Polycystic liver disease, Polycystic ovary syndrome, Polydactyly, Renal agenesis, Renal cyst, Renal dysplasia, Renal hypoplasia, Sclerocornea, Situs inversus, Syndactyly of the toes, Syndromic microphthalmia, Talipes, True hermaphroditism, Postaxial hand polydactyly, Urethral atresiaView all (33 more) |
|
832
|
|
|
CWF19 like cell cycle control factor 1 |
C19L1, SCAR17, hDrn1 |
Agenesis of corpus callosum, Spinocerebellar ataxia, Cerebellar ataxia, Cerebellar hypoplasia, Developmental delay, Dysarthria, Horizontal nystagmus, Mental retardation, Oculomotor apraxia, Oculovestibuloauditory syndrome, Synophrys |
|
833
|
|
|
Coiled-coil domain containing 91 |
HSD8, p56 |
|
|
834
|
|
|
Choline dehydrogenase |
- |
|
|
835
|
|
|
Chondroitin sulfate N-acetylgalactosaminyltransferase 2 |
CHGN2, ChGn-2, GALNACT-2, GALNACT2, PRO0082, beta4GalNAcT |
|
|
836
|
|
|
Cell division cycle associated 7 like |
JPO2, R1, RAM2 |
|
|
837
|
|
|
CDC42 binding protein kinase gamma |
DMPK2, HSMDPKIN, KAPPA-200, MRCKG, MRCKgamma |
|
|
838
|
|
|
Capping protein regulator and myosin 1 linker 1 |
CARMIL, CARMIL1a, LRRC16, LRRC16A, dJ501N12.1, dJ501N12.5 |
Anorexia, Coronary heart disease, Development disorder, Diabetes, Diabetes mellitus, Gout, Gouty arthritis, Lung carcinoma, Lupus erythematosus, Obsessive-compulsive disorder, Schizophrenia, Stroke |
|
839
|
|
|
Chromodomain helicase DNA binding protein 7 |
CRG, HH5, IS3, KAL5 |
Absence of septum pellucidum, Alopecia, Anemia, Aneurysm of aortic arch, Anxiety disorder, Aortic coarctation, Aqueductal stenosis, Asymmetric crying face association, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Charge syndrome, Choanal atresia, Cleft palate and bilateral cleft lip, Congenital atresia of pulmonary artery, Congenital camptodactyly, Congenital coloboma of iris, Congenital epicanthus, Congenital exomphalos, Breast hypoplasia, Hypoplasia of the ovary, Congenital ocular coloboma, Congenital omphalocele, Congenital sensorineural hearing loss, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Dolichocephaly, Double outlet right ventricle, Duodenal atresia, Dwarfism, Dysarthria, Dysmorphic features, Dysphagia, Eosinophilia, Erectile dysfunction, Esophageal atresia, Exfoliative dermatitis, Facial paralysis, Female hypogonadism syndrome, Fundus coloboma, Gastroesophageal reflux disease, Gonadotropin deficiency, Gynecomastia, Hearing loss, Heart septal defects, Holoprosencephaly, Horseshoe kidney, Hydrocephalus, Hydronephrosis, Hypogonadism, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism with or without anosmia, Hypopituitarism, Hypoplasia of corpus callosum, Hypoplasia of thumb, Hypothyroidism, Ichthyosis, Immunologic deficiency syndromes, Imperforate anus, Interrupted aortic arch, Isolated somatotropin deficiency, Kallmann syndrome, Laryngeal hypoplasia, Laryngomalacia, Lobar holoprosencephaly, Lymphoma, Lymphopenia, Mental depression, Mental retardation, Microcephaly, Micrognathism, Micropenis, Microphthalmos, Microstomia, Microtia, Mirror movements, Movement disorders, Multiple congenital anomalies, Myopia, Neck webbing, Nephrotic syndrome, Non-obstructive azoospermia, Normosmic congenital hypogonadotropic hypogonadism, Nystagmus, Obesity, Obsessive-compulsive disorder, Omenn syndrome, Optic atrophy, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Parathyroid hypoplasia, Patent ductus arteriosus, Penis agenesis, Physiologic amenorrhea, Posteriorly rotated ear, Prostatic neoplasms, Prostate cancer, Ptosis, Pulmonary stenosis, Renal agenesis, Renal hypoplasia, Retinal coloboma, Scoliosis, Secondary physiologic amenorrhea, Severe combined immunodeficiency disease, Skeletal dysplasia, Somatotropin deficiency, Strabismus, Syndactyly, Syndromic microphthalmia, Talipes, Testicular hypogonadism, Tetralogy of fallot, Thyroiditis, Tracheal stenosis, Transposition of great vessels, Ventricular septal defect, Vesicoureteral refluxView all (109 more) |
|
840
|
|
|
Cell division cycle 37 like 1, HSP90 cochaperone |
CDC37B, HARC |
|
