68
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|
|
OFD1 centriole and centriolar satellite protein |
71-7A, CXorf5, JBTS10, RP23, SGBS2 |
Curated: Bifid nail, Congenital anomalies of the kidney and urinary tract, Ciliary dyskinesia, Ciliopathy, Coach syndrome, Connective tissue disease, Desbuquois syndrome, Aplasia of the vermis, Joubert syndrome, Orofaciodigital syndrome, Osteoporosis, Otopalatodigital syndrome, Polydactyly, Polymicrogyria, Retinitis pigmentosa, Simpson-golabi-behmel syndrome, Spastic paraplegia, Spondyloepiphyseal dysplasia, OFD1-related ciliopathy
Unreviewed: Acquired Porencephaly, Agenesis Of Corpus Callosum, Alopecia, Anodontia, Arachnoid cyst, Asplenia, Asthenozoospermia, Asthma, Autism, Bardet-Biedl Syndrome, Brachydactyly, Brain malformation, Bronchiectasis, Calcinosis, Camptodactyly of fingers, Carcinogenesis, Cataract, Cerebellar vermis agenesis, Choanal Atresia, Ciliopathies, Cleft palate, Clinodactyly, Congenital abnormalities, Congenital Clubfoot, Congenital Epicanthus, Congenital heart defects, Congenital Hypoplasia Of Penis, Congenital Pectus Excavatum, Corneal Dystrophy, Coronary Heart Disease, Craniofacial abnormalities, Cryptorchidism, Cystic Kidney Disease, Dandy-Walker Syndrome, Dental Enamel Hypoplasia, Development Disorder, Developmental Delay, Developmental disability, Developmental dysplasia of the hip, Diabetes Mellitus, Disorder Of Eye, Dolichocephaly, Dwarfism, Esotropia, Exocrine pancreatic insufficiency, Frontal bossing, Gastric Cancer, Glaucoma, Hearing Loss, Hearing loss with stapes fixation, High palate, Hydrocephalus, Hydronephrosis, Hyperinsulinism, Hypertension, Hypodontia, Hypogonadism, Hypothalamic Hamartomas, Kartagener Syndrome, Keratoconus, Kidney disease, Language development disorders, Leber congenital amaurosis, Liver Cyst, Liver Fibrosis, Lung Diseases, Macrocephaly, Macrostomia, Malformation of cortical development, Mental retardation, Microcephaly, Micrognathism, Monoclonal Gammapathies, Movement Disorders, Multicystic renal dysplasia, Multiple myeloma, Nasal polyposis, Neuronal Heterotopia, Nystagmus, Obesity, Odontogenic Tumor, Optic Atrophy, Osteofibrous Dysplasia, Otitis media, Oto-Palato-digital syndrome, Ovarian Cysts, Pancreatic Cyst, Papillary Craniopharyngioma, Paroxysmal dystonia, Pena Shokeir syndrome, Penis Agenesis, Periventricular nodular heterotopia, Polycystic kidney disease, Polydactyly Of Toes, Porencephalic cyst, Postaxial hand polydactyly, Posteriorly Rotated Ear, Radial Polydactyly, Renal agenesis, Renal Insufficiency, Retinal degeneration, Retinitis Pigmentosa, Retinitis Pigmentosa, X-Linked, Rhinitis, Rod-cone dystrophy, Scaphocephaly, Scoliosis, Simpson-Golabi-Behmel Syndrome, Sinusitis, Situs Inversus, Spade-Like Hand, Spinocerebellar ataxia, Syndactyly, Syndactyly of fingers, Tarsal Coalition, Vitiligo
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69
|
|
|
OFD1 pseudogene 10 Y-linked |
OFD1P10, OFD1PY10, OFDYP10 |
Curated: N/A
Unreviewed: N/A
|
70
|
|
|
OFD1 pseudogene 11 Y-linked |
OFD1P11, OFD1PY11, OFDYP11 |
Curated: N/A
Unreviewed: N/A
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