1605
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Centrosomal protein 20 |
C16orf63, FOPNL, FOR20, PHSECRG2 |
Curated: Multiple myeloma, Pelvic organ prolapse, Psoriasis
Unreviewed: Ciliopathies, Diabetes, Diabetes Mellitus, Endometrial Cancer, Endometrial carcinoma, Hypertension, Ischemic Stroke, Liver carcinoma, Merkel cell carcinoma, Orofaciodigital syndrome, Skin carcinoma, Stroke
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1608
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Centrosomal protein 290 |
3H11Ag, BBS14, CT87, JBTS5, LCA10, MKS4, NPHP6, POC3, SLSN6, rd16 |
Curated: Arima syndrome, Hemolytic uremic syndrome, Bardet-biedl syndrome, Blindness, Cone-rod dystrophy, Congenital kidney anomaly, Congenital disorder of glycosylation, Congenital neurologic anomalies, Cystic kidney disease, Desbuquois syndrome, Encephalocele, Aplasia of the vermis, Global developmental delay, Intellectual developmental disorder, Joubert syndrome, Kidney disease, Leber congenital amaurosis, Meckel-gruber syndrome, Micrognathism, Nephronophthisis, Nystagmus, Optic atrophy, Polycystic kidney disease, Retinitis pigmentosa, Rod-cone dystrophy, Senior-loken syndrome, Spastic ataxia, Stuve-wiedemann syndrome, CEP290-related ciliopathy
Unreviewed: Alstrom Syndrome, Anencephaly, Arima Syndrome, Asplenia, Atrial Septal Defect, Atrioventricular septal defect, Autism, Bardet-Biedl Syndrome, Cataract, Cerebellar vermis agenesis, Choroideremia, Ciliopathies, Ciliopathy, Color vision deficiency, Cone dystrophy, Congenital blindness, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital Hepatic Fibrosis, Congenital Hypoplasia Of Penis, Congenital Meningocele, Congenital nystagmus, Congenital ocular coloboma, Congestive Heart Failure, Cryptorchidism, Cystic Kidney Disease, Cystic liver disease, Dandy-Walker Syndrome, Developmental Delay, Developmental disability, Diastrophic Dysplasia, Disorder Of Eye, Double Ureter, Down syndrome, Drachtman Weinblatt Sitarz syndrome, Dwarfism, Fibrosis Of Pancreas, Foot Polydactyly, Fundus Coloboma, Growth disorder, Hemiplegia/hemiparesis, Hemochromatosis, Hepatocellular carcinoma, Hereditary Leber Optic Atrophy, Hirschsprung Disease, Hydrocephalus, Hypertension, Hypogonadism, Hypogonadotropic hypogonadism, Hypoplasia Of Corpus Callosum, Hypoplasia of the ovary, Joubert Syndrome, Joubert Syndrome With Oculorenal Defect, Kallmann syndrome, Keratoconus, Keratosis Follicularis, Kidney Disease, Leber Congenital Amaurosis, Liver Fibrosis, Lobar Holoprosencephaly, Macular dystrophy, Male Pseudohermaphroditism, Malformation of cortical development, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Microcephaly, Microcornea, Microphthalmos, MOHR-TRANEBJAERG SYNDROME, Multicystic renal dysplasia, Nephrotic Syndrome, Obesity, Occipital Encephalocele, Oculocerebrorenal syndrome, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Optic Atrophy, Orofaciodigital syndrome, Pancreatic Cyst, Polycystic liver disease, Polydactyly, Polydactyly Of Toes, Postaxial hand polydactyly, Premature Menopause, Ptosis, Renal cyst, Renal dysplasia and retinal aplasia, Renal Insufficiency, Retinal coloboma, Retinal degeneration, Retinal detachment, Retinal Diseases, Retinal Dystrophy, Retinitis Pigmentosa, Sclerocornea, Scoliosis, Senior-Loken Syndrome, Situs Inversus, Sleep Apnea, Speech Disorders, Strabismus, Syndactyly of fingers, Syndromic microphthalmia, Talipes, Trichohepatoenteric Syndrome, True Hermaphroditism, Urethral atresia, Ventricular septal defect, Visual disorder
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