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Autosomal recessive inheritance

Information related to Autosomal recessive inheritance

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, Autosomal recessive bestrophinopathy, Worth syndrome, Autosomal dominant porencephaly type I, Autosomal recessive multiple epiphyseal dysplasia, Prevention of autosomal recessive disorders, Autosomal recessive axonal neuropathy with neuromyotonia, 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, Craniometaphyseal dysplasia, Autosomal dominant partial epilepsy with auditory features, Autosomal recessive spastic ataxia of Charlevoix-Saguenay, Cochleosaccular degeneration with progressive cataracts, 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, CADASIL, Monilethrix, 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, Situs ambiguus, Hair loss, Titin, Craniosynostosis, Hydrocephalus, Genetic linkage, تاريخ_الهندسة_الرياضية, Stamboom_Christina_van_Oranje-Nassau_(1947), Effects_of_Hurricane_Matthew_in_Haiti, JYP_Entertainment, Food_Network_Challenge, Братство_(фильм,_2019), Dietrich_Mateschitz

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, Autosomal recessive bestrophinopathy, Worth syndrome, Autosomal dominant porencephaly type I, Autosomal recessive multiple epiphyseal dysplasia, Prevention of autosomal recessive disorders, Autosomal recessive axonal neuropathy with neuromyotonia, 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, Craniometaphyseal dysplasia, Autosomal dominant partial epilepsy with auditory features, Autosomal recessive spastic ataxia of Charlevoix-Saguenay, Cochleosaccular degeneration with progressive cataracts, 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, CADASIL, Monilethrix, 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, Situs ambiguus, Hair loss, Titin, Craniosynostosis, Hydrocephalus, Genetic linkage, تاريخ_الهندسة_الرياضية, Stamboom_Christina_van_Oranje-Nassau_(1947), Effects_of_Hurricane_Matthew_in_Haiti, JYP_Entertainment, Food_Network_Challenge, Братство_(фильм,_2019), Dietrich_Mateschitz, العلاقات_البريطانية_النمساوية, Big_E_Langston, Bhutan, KAKC, Yamaha_YZF-R3, تنظيم_تقنية_النانو, Worlds_Finest, Sukyatno_Nugroho, The_Greatest_Love, Bombeo_láser, National_Review, AEW_Fight_for_the_Fallen, Zulhijah, Doraemon_-_Il_film:_Le_avventure_di_Nobita_e_dei_cinque_esploratori, Rissanda_Putri, Barthélemy_de_Theux_de_Meylandt, Соланильос-дель-Эстремо, Peñón_de_Alhucemas, Comando_delle_forze_speciali_dell'Esercito, マヤ暦, Green_spaces_and_walkways_in_Aberdeen, Liang_Jun_(pengemudi_traktor), Batalyon_Zeni_Tempur_9, Margaret_Mead, Eparquía_de_Sokal-Zhovkva, 四国旅客鉄道, Sarhad_(flod), Luigi_Chiarelli, Fikar_W._Eda, Saint-Jean-sur-Veyle, Yehezkiel_4, Tiga_Inti_Utama, Kalong_besar, ウインフルブルーム, Kabupaten_Landak, PlayStation_TV, Смирнов_Валерій_Олександрович, Campeonato_nacional_de_Estados_Unidos_1888, ペペ_(映画), عبد_العزيز_العروي, Landvetter, Люм'єр_(кінотеатр,_Івано-Франківськ), Katharine_Ross, Regio_II_Caelimontium, متغير_العملية, Outline_of_the_State_of_Palestine, Jean-Baptiste_Hugues, Nevada_State_Route_562, ラッシュ時, فيكتوريا_مارينوفا, Песчаный_Умёт, MIN_Timpik, Kleptoparasitism, Halterofilismo_nos_Jogos_Olímpicos_de_Verão_da_Juventude_de_2010_-_Até_62_kg_masculino, List_of_Dr._Slump_films, Джаниев,_Ровшан_Рафик_оглы, President's_House_(University_of_Florida), Red_Wings_Airlines_Flight_9268, ECAM_LaSalle, Olivier_De_Schutter

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