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Autosome, Autosomal recessive cerebellar ataxia type 1, Autosomal dominant cerebellar ataxia, Autosomal dominant Charcot–Marie–Tooth disease type 2 with giant axons, Autosomal recessive polycystic kidney disease, Autosomal dominant polycystic kidney disease, Autosomal dominant GTP cyclohydrolase I deficiency, Worth syndrome, Autosomal recessive bestrophinopathy, Autosomal dominant porencephaly type I, Autosomal recessive multiple epiphyseal dysplasia, Autosomal recessive axonal neuropathy with neuromyotonia, Prevention of autosomal recessive disorders, Autosomal dominant leukodystrophy with autonomic disease, Alwadei syndrome, Autosomal recessive isolated ectopia lentis, Autosomal recessive cerebellar ataxia, Autosomal dominant multiple pterygium syndrome, Woolly hair autosomal recessive, Autosomal dominant cerebellar ataxia, deafness, and narcolepsy, Autosomal dominant partial epilepsy with auditory features, Craniometaphyseal dysplasia, Cochleosaccular degeneration with progressive cataracts, Autosomal recessive spastic ataxia of Charlevoix-Saguenay, Tetra-amelia syndrome, Autosomal dominant nocturnal frontal lobe epilepsy, Trisomy, Medullary cystic kidney disease, CARASIL, Polycystic kidney disease 3 (autosomal dominant), Autosomal dominant hypophosphatemic rickets, Genealogical DNA test, Autosomal recessive GTP cyclohydrolase I deficiency, Hypohidrotic ectodermal dysplasia, Monilethrix, CADASIL, Bethlem myopathy, Tyrosine hydroxylase deficiency, Microcephaly lymphoedema chorioretinal dysplasia, Robinow syndrome, Familial exudative vitreoretinopathy
Nonsyndromic deafness, CHAMP1-associated intellectual disability syndrome, Retinitis pigmentosa, Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome, Ichthyosis, Dominance (genetics), Genetic disorder, Chondrodysplasia punctata, Photic sneeze reflex, Osteopetrosis, Limb–girdle muscular dystrophy, Mandibulofacial dysostosis-microcephaly syndrome, Ichthyosis vulgaris, Distal renal tubular acidosis, Palmoplantar keratoderma, TNF receptor associated periodic syndrome, Hypogammaglobulinemia, Sideroblastic anemia, Distal spinal muscular atrophy type 1, Pendred syndrome, Otoferlin, Aneuploidy, Ectrodactyly, Microcephaly, Hereditary spastic paraplegia, Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations, Optic neuropathy, FXR2, Rhizomelic chondrodysplasia punctata, DiGeorge syndrome, Mitral valve prolapse, Congenital cataract, Kinky hair, Multicystic dysplastic kidney, Aplasia cutis congenita, Congenital nephrotic syndrome, Adrenoleukodystrophy, Hair loss, Situs ambiguus, Titin, Craniosynostosis, Hydrocephalus, Genetic linkage, Terumasa_Kin, Departemen_Pertahanan_Amerika_Serikat, Park_Eun-bin, List_of_rail_accidents_in_the_Philippines, ألعاب_البحر_الأبيض_المتوسط_2022, Academia_Colombiana_de_la_Lengua, NGC_1998
Autosome, Autosomal recessive cerebellar ataxia type 1, Autosomal dominant cerebellar ataxia, Autosomal dominant Charcot–Marie–Tooth disease type 2 with giant axons, Autosomal recessive polycystic kidney disease, Autosomal dominant polycystic kidney disease, Autosomal dominant GTP cyclohydrolase I deficiency, Worth syndrome, Autosomal recessive bestrophinopathy, Autosomal dominant porencephaly type I, Autosomal recessive multiple epiphyseal dysplasia, Autosomal recessive axonal neuropathy with neuromyotonia, Prevention of autosomal recessive disorders, Autosomal dominant leukodystrophy with autonomic disease, Alwadei syndrome, Autosomal recessive isolated ectopia lentis, Autosomal recessive cerebellar ataxia, Autosomal dominant multiple pterygium syndrome, Woolly hair autosomal recessive, Autosomal dominant cerebellar ataxia, deafness, and narcolepsy, Autosomal dominant partial epilepsy with auditory features, Craniometaphyseal dysplasia, Cochleosaccular degeneration with progressive cataracts, Autosomal recessive spastic ataxia of Charlevoix-Saguenay, Tetra-amelia syndrome, Autosomal dominant nocturnal frontal lobe epilepsy, Trisomy, Medullary cystic kidney disease, CARASIL, Polycystic kidney disease 3 (autosomal dominant), Autosomal dominant hypophosphatemic rickets, Genealogical DNA test, Autosomal recessive GTP cyclohydrolase I deficiency, Hypohidrotic ectodermal dysplasia, Monilethrix, CADASIL, Bethlem myopathy, Tyrosine hydroxylase deficiency, Microcephaly lymphoedema chorioretinal dysplasia, Robinow syndrome, Familial exudative vitreoretinopathy, Nonsyndromic deafness, CHAMP1-associated intellectual disability syndrome, Retinitis pigmentosa, Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome, Ichthyosis, Dominance (genetics), Genetic disorder, Chondrodysplasia punctata, Photic sneeze reflex, Osteopetrosis, Limb–girdle muscular dystrophy, Mandibulofacial dysostosis-microcephaly syndrome, Ichthyosis vulgaris, Distal renal tubular acidosis, Palmoplantar keratoderma, TNF receptor associated periodic syndrome, Hypogammaglobulinemia, Sideroblastic anemia, Distal spinal muscular atrophy type 1, Pendred syndrome, Otoferlin, Aneuploidy, Ectrodactyly, Microcephaly, Hereditary spastic paraplegia, Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations, Optic neuropathy, FXR2, Rhizomelic chondrodysplasia punctata, DiGeorge syndrome, Mitral valve prolapse, Congenital cataract, Kinky hair, Multicystic dysplastic kidney, Aplasia cutis congenita, Congenital nephrotic syndrome, Adrenoleukodystrophy, Hair loss, Situs ambiguus, Titin, Craniosynostosis, Hydrocephalus, Genetic linkage, Terumasa_Kin, Departemen_Pertahanan_Amerika_Serikat, Park_Eun-bin, List_of_rail_accidents_in_the_Philippines, ألعاب_البحر_الأبيض_المتوسط_2022, Academia_Colombiana_de_la_Lengua, NGC_1998, Aureliu_Ciocoi, Daftar_Bupati_Wakatobi, Padatan_amorf, Куплеваский,_Николай_Осипович, Kawasan_Tadahan_Air_Barat_(Singapura), شمة_الكواري, Active_Directory, Радиальная_скорость, SMP_Labschool_Kebayoran, Man_Is_Not_a_Bird, Меклин,_Наталья_Фёдоровна, بيير_رولان, 2007_Gibraltar_general_election, Pulau_Sebatik, Juventus_F.C., Ilha_de_Lagos, Miracle_Mineral_Supplement, Cop_and_a_Half, ラブドール, Sevilla, Doppiatore, Торрекуадрада-де-Молина, Giovanna_d'Aragona,_Duchess_of_Amalfi, Чирвинский,_Владимир_Николаевич, العلاقات_التوفالية_الكورية_الشمالية, Yakobus_1, Mana_Iwabuchi, Jonathan_Frakes, مادة_مظللة, Aceh_Medal, Bertrand's_postulate, Isola_di_Caprera_(traghetto), Mahon_Port, Энрике_(король_Португалии), Richard_Codey, Independent_Regionalist_Party, Beautiful_Days_(serial_TV), Ham_(tokoh_Alkitab), Pembukaan_catur, سعدي_(بعلبك), Zhu_Bajie, Uncle_Maddio's_Pizza_Joint, Diócesis_de_Bandung, Багратиони,_Вахтанг, Pengejaran_Jendral_Blue, Android_Donut, Santuario_de_Nuestra_Señora_del_Rosario_(Hellín), César_Gabriel_de_Choiseul-Praslin, Prasasti_Sebna, Studio_Alam_TVRI, Bobby_Lee, List_of_Regia_Aeronautica_aircraft_used_in_World_War_II, Rudy_Yakym, Лаврский_переулок_(Москва), フナ, Bayur, جون_براون_(تاجر), Mangham,_Louisiana, تاريخ_الهندسة_الرياضية, Stamboom_Christina_van_Oranje-Nassau_(1947)