Also known as: COCHLEOSACCULAR degeneration with progressive cataracts, Cochleosaccular Degeneration, Cochleosaccular Degeneration of the inner Ear with progressive cataracts, Cochleosaccular degeneration of the inner ear and progressive cataracts
Also known as: CSA, Cockayne syndrome A, Cockayne syndrome caused by mutation in ERCC8, Cockayne syndrome classic form, Cockayne syndrome classical, Cockayne syndrome type 1, Cockayne syndrome type A, Cockayne syndrome type I, Cockayne syndrome type a, Cockayne syndrome, type A, ERCC8 Cockayne syndrome
Also known as: CSB, Cockayne syndrome B, Cockayne syndrome type 2, Cockayne syndrome type B, Cockayne syndrome type II, Cockayne syndrome, type B
Also known as: Cockayne syndrome type 3, Cockayne syndrome type C, Cockayne syndrome type III, Cockayne syndrome, type III
Also known as: cocoon syndrome, fetal encasement syndrome, foetal encasement syndrome
Also known as: CODAS syndrome, cerebral, ocular, dental, auricular, and skeletal anomalies syndrome, cerebral, ocular, dental, auricular, and skeletal syndrome, cerebro-oculo-dento-auriculo-skeletal syndrome, cerebrooculodentoauriculoskeletal syndrome
Also known as: COQ10D1, COQ2 coenzyme Q10 deficiency, CoQ deficiency 1, Coq10 deficiency, primary, 1, coenzyme Q deficiency 1, coenzyme Q10 deficiency caused by mutation in COQ2, coenzyme Q10 deficiency, primary, 1, coenzyme Q10 deficiency, primary, type 1, ubiquinone deficiency 1
Also known as: COQ10D3, PDSS2 coenzyme Q10 deficiency, coenzyme Q10 deficiency caused by mutation in PDSS2, coenzyme Q10 deficiency, primary, 3, coenzyme Q10 deficiency, primary, type 3
Also known as: COQ10D9
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