Autosomal set

Autosome, Autosomal dominant leukodystrophy with autonomic disease, Autosomal recessive cerebellar ataxia type 1, Autosomal dominant cerebellar ataxia, Autosomal dominant Charcot–Marie–Tooth disease type 2 with giant axons, Autosomal dominant polycystic kidney disease, Autosomal recessive polycystic kidney disease, Bartsocas-Papas syndrome, Autosomal dominant GTP cyclohydrolase I deficiency, Autosomal recessive bestrophinopathy, Worth syndrome, Prevention of autosomal recessive disorders, Autosomal dominant porencephaly type I, Autosomal recessive axonal neuropathy with neuromyotonia, Autosomal recessive multiple epiphyseal dysplasia, Alwadei syndrome, Autosomal recessive isolated ectopia lentis, Autosomal recessive cerebellar ataxia, Autosomal dominant multiple pterygium syndrome, Autosomal dominant cerebellar ataxia, deafness, and narcolepsy, Autosomal recessive spastic ataxia of Charlevoix-Saguenay, Autosomal dominant partial epilepsy with auditory features, Woolly hair autosomal recessive, Craniometaphyseal dysplasia, Cochleosaccular degeneration with progressive cataracts, Autosomal dominant nocturnal frontal lobe epilepsy, Tetra-amelia syndrome, Trisomy, CARASIL, Medullary cystic kidney disease, Polycystic kidney disease 3 (autosomal dominant), Autosomal recessive GTP cyclohydrolase I deficiency, Autosomal dominant hypophosphatemic rickets, Hypohidrotic ectodermal dysplasia, Genealogical DNA test, CADASIL, Monilethrix, Bethlem myopathy, Microcephaly lymphoedema chorioretinal dysplasia, Tyrosine hydroxylase deficiency, Robinow syndrome

Nonsyndromic deafness, Familial exudative vitreoretinopathy, Retinitis pigmentosa, Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome, Osteopetrosis, Chondrodysplasia punctata, Ichthyosis, Genetic disorder, Dominance (genetics), Photic sneeze reflex, Limb–girdle muscular dystrophy, Mandibulofacial dysostosis-microcephaly syndrome, Ichthyosis vulgaris, Palmoplantar keratoderma, Distal renal tubular acidosis, TNF receptor associated periodic syndrome, Distal spinal muscular atrophy type 1, Hypogammaglobulinemia, Sideroblastic anemia, Pendred syndrome, Otoferlin, Aneuploidy, Ectrodactyly, Microcephaly, Hereditary spastic paraplegia, CHAMP1-associated intellectual disability syndrome, Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations, Optic neuropathy, FXR2, Rhizomelic chondrodysplasia punctata, DiGeorge syndrome, Mitral valve prolapse, Congenital cataract, Multicystic dysplastic kidney, Kinky hair, Aplasia cutis congenita, Congenital nephrotic syndrome, Adrenoleukodystrophy, Titin, Situs ambiguus, Hair loss, Craniosynostosis, Hydrocephalus, Genetic linkage, Onze-Lieve-Vrouw-Troost_der_Kleine_Kinderen, Маллет_(лунный_кратер), العلاقات_الأوكرانية_العراقية, Guerre_di_religione_in_Europa, ألطاف_حسين_(لاعب_كريكت), ジェイコムウエスト

Autosome, Autosomal dominant leukodystrophy with autonomic disease, Autosomal recessive cerebellar ataxia type 1, Autosomal dominant cerebellar ataxia, Autosomal dominant Charcot–Marie–Tooth disease type 2 with giant axons, Autosomal dominant polycystic kidney disease, Autosomal recessive polycystic kidney disease, Bartsocas-Papas syndrome, Autosomal dominant GTP cyclohydrolase I deficiency, Autosomal recessive bestrophinopathy, Worth syndrome, Prevention of autosomal recessive disorders, Autosomal dominant porencephaly type I, Autosomal recessive axonal neuropathy with neuromyotonia, Autosomal recessive multiple epiphyseal dysplasia, Alwadei syndrome, Autosomal recessive isolated ectopia lentis, Autosomal recessive cerebellar ataxia, Autosomal dominant multiple pterygium syndrome, Autosomal dominant cerebellar ataxia, deafness, and narcolepsy, Autosomal recessive spastic ataxia of Charlevoix-Saguenay, Autosomal dominant partial epilepsy with auditory features, Woolly hair autosomal recessive, Craniometaphyseal dysplasia, Cochleosaccular degeneration with progressive cataracts, Autosomal dominant nocturnal frontal lobe epilepsy, Tetra-amelia syndrome, Trisomy, CARASIL, Medullary cystic kidney disease, Polycystic kidney disease 3 (autosomal dominant), Autosomal recessive GTP cyclohydrolase I deficiency, Autosomal dominant hypophosphatemic rickets, Hypohidrotic ectodermal dysplasia, Genealogical DNA test, CADASIL, Monilethrix, Bethlem myopathy, Microcephaly lymphoedema chorioretinal dysplasia, Tyrosine hydroxylase deficiency, Robinow syndrome, Nonsyndromic deafness, Familial exudative vitreoretinopathy, Retinitis pigmentosa, Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome, Osteopetrosis, Chondrodysplasia punctata, Ichthyosis, Genetic disorder, Dominance (genetics), Photic sneeze reflex, Limb–girdle muscular dystrophy, Mandibulofacial dysostosis-microcephaly syndrome, Ichthyosis vulgaris, Palmoplantar keratoderma, Distal renal tubular acidosis, TNF receptor associated periodic syndrome, Distal spinal muscular atrophy type 1, Hypogammaglobulinemia, Sideroblastic anemia, Pendred syndrome, Otoferlin, Aneuploidy, Ectrodactyly, Microcephaly, Hereditary spastic paraplegia, CHAMP1-associated intellectual disability syndrome, Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations, Optic neuropathy, FXR2, Rhizomelic chondrodysplasia punctata, DiGeorge syndrome, Mitral valve prolapse, Congenital cataract, Multicystic dysplastic kidney, Kinky hair, Aplasia cutis congenita, Congenital nephrotic syndrome, Adrenoleukodystrophy, Titin, Situs ambiguus, Hair loss, Craniosynostosis, Hydrocephalus, Genetic linkage, Onze-Lieve-Vrouw-Troost_der_Kleine_Kinderen, Маллет_(лунный_кратер), العلاقات_الأوكرانية_العراقية, Guerre_di_religione_in_Europa, ألطاف_حسين_(لاعب_كريكت), ジェイコムウエスト, Stasiun_Gombong, Lil_Jon, العلاقات_الباكستانية_البنينية, Angel's_Friends, Siobhan_Marsden, جاذبية_سطحية, 第9回NHK紅白歌合戦, Новый_город_(Ульяновск), 横浜市立市沢小学校, Fausto_Romero-Miura, 1972_у_кіно, العلاقات_الأردنية_الكورية_الشمالية, Frontera_entre_Tanzania_y_la_República_Democrática_del_Congo, Charlotte_Church, Sri_Lankan_cricket_team_in_Australia_in_2007–08, Shin_Byung-hyun, Skåne-Tranås, Leonor_Álvarez_de_Toledo_y_Colonna, Initialization_vector, List_of_active_Italian_Navy_ships, الحارت_(آيت_حمو), أدريان_شيلي, Stasiun_Rikuzen-Akasaki, إدوارد_بيلامي, Список_министров_экономики_и_финансов_Италии, Kevin_Hart:_What_Now?_(The_Mixtape_Presents_Chocolate_Droppa), Emping, Tokyo, Standing_on_the_Edge_of_the_Noise, Tranvía_de_Orán, 第33回NHK紅白歌合戦, 阪神タクシー, Sofia_(530-601), Brigata_di_reazione_rapida_multinazionale, 2002_ABC_Under-18_Championship, Joaquín_de_Eleta, Dermot_Kelly_(actor), Национальная_служба_безопасности_Бангладеш, Världsmästerskapen_i_skidskytte_1982, الحزب_الديمقراطي_الياباني, الدوري_البلجيكي_الدرجة_الأولى_1912–13, Шунь, Leonor_Álvarez_de_Toledo_y_Osorio, Kegemukan, Fins_voetbalelftal_(vrouwen), Tiahuanaco_(poblado), Proses_Frank–Caro, العلاقات_الهندية_اليونانية, 103rd_Street_(Rosemoor)_station, Simbol_Islam, كأس_ويلز_1955–56, Hula_Fulla_Dance, Coba, Уваров,_Николай_Митрофанович, Archivio_di_Stato_di_Perugia, Catur_pada_Pekan_Olahraga_Nasional_XIX_–_Kilat_beregu_putri, Stasiun_Rawa_Buntu, Contrôleur_général_des_lieux_de_privation_de_liberté, Соловьёв,_Леонид_Николаевич, Stasiun_Jinniuhu