Recessive trait

Dominance (genetics), Autosomal recessive multiple epiphyseal dysplasia, X-linked recessive inheritance, Recessive Pied budgerigar mutation, Autosomal recessive polycystic kidney disease, Autosomal recessive cerebellar ataxia type 1, Prevention of autosomal recessive disorders, X-linked recessive chondrodysplasia punctata, Autosomal recessive bestrophinopathy, Bartsocas-Papas syndrome, X-linked recessive hypoparathyroidism, Autosomal recessive axonal neuropathy with neuromyotonia, Autosomal recessive cerebellar ataxia, Hereditary carrier, Lethal allele, Alwadei syndrome, Autosomal recessive isolated ectopia lentis, Autosomal recessive spastic ataxia of Charlevoix-Saguenay, Woolly hair autosomal recessive, Tetra-amelia syndrome, CARASIL, DOOR syndrome, Lamellar ichthyosis, Autosomal recessive GTP cyclohydrolase I deficiency, Genetic disorder, X-linked complicated corpus callosum dysgenesis, Hypohidrotic ectodermal dysplasia, Barytonesis, Tyrosine hydroxylase deficiency, Robinow syndrome, Cutis laxa, Ichthyosis, Adducted thumb syndrome, Otoferlin, Craniometaphyseal dysplasia, Zygosity, X-linked ichthyosis, Larsen syndrome, Oculodentodigital dysplasia, Epidermolysis bullosa dystrophica, Monilethrix

Nonsyndromic deafness, Pseudoxanthoma elasticum, Osteopetrosis, Familial exudative vitreoretinopathy, Spinocerebellar ataxia, Pendred syndrome, Distal spinal muscular atrophy type 1, Multicentric carpotarsal osteolysis syndrome, Methemoglobinemia, Hereditary spastic paraplegia, Alport syndrome, Pelizaeus–Merzbacher disease, Distal renal tubular acidosis, Rhizomelic chondrodysplasia punctata, Hypogammaglobulinemia, Hereditary sensory and autonomic neuropathy, Microcephaly, Ectrodactyly, Klippel–Feil syndrome, Optic neuropathy, Aplasia cutis congenita, Charcot–Marie–Tooth disease, Aarskog–Scott syndrome, Benign infantile epilepsy, Nephrogenic diabetes insipidus, Kinky hair, Multicystic dysplastic kidney, Congenital nephrotic syndrome, Hair loss, Benign familial neonatal seizures, Hydrocephalus, Dandy–Walker malformation, Hay–Wells syndrome, B Positive, Richard_J._Berry, 上峰町, Симфонія_№_37_(Моцарт), بيت_أبو_مرعى_(أرحب), Tikus_Desa_dan_Tikus_Kota, Нападение_в_джунглях, The_Miraculous_Draught_of_Fishes_(Jordaens), Mi_wonton, Istana_Stockholm, Kimberley_Echo, ショーン・チャコーン, Judo, Dodge_50_Series, SMA_Negeri_8_Medan, Кабрал_ди_Мелу_Нету,_Жуан, Currys_Digital

Dominance (genetics), Autosomal recessive multiple epiphyseal dysplasia, X-linked recessive inheritance, Recessive Pied budgerigar mutation, Autosomal recessive polycystic kidney disease, Autosomal recessive cerebellar ataxia type 1, Prevention of autosomal recessive disorders, X-linked recessive chondrodysplasia punctata, Autosomal recessive bestrophinopathy, Bartsocas-Papas syndrome, X-linked recessive hypoparathyroidism, Autosomal recessive axonal neuropathy with neuromyotonia, Autosomal recessive cerebellar ataxia, Hereditary carrier, Lethal allele, Alwadei syndrome, Autosomal recessive isolated ectopia lentis, Autosomal recessive spastic ataxia of Charlevoix-Saguenay, Woolly hair autosomal recessive, Tetra-amelia syndrome, CARASIL, DOOR syndrome, Lamellar ichthyosis, Autosomal recessive GTP cyclohydrolase I deficiency, Genetic disorder, X-linked complicated corpus callosum dysgenesis, Hypohidrotic ectodermal dysplasia, Barytonesis, Tyrosine hydroxylase deficiency, Robinow syndrome, Cutis laxa, Ichthyosis, Adducted thumb syndrome, Otoferlin, Craniometaphyseal dysplasia, Zygosity, X-linked ichthyosis, Larsen syndrome, Oculodentodigital dysplasia, Epidermolysis bullosa dystrophica, Monilethrix, Nonsyndromic deafness, Pseudoxanthoma elasticum, Osteopetrosis, Familial exudative vitreoretinopathy, Spinocerebellar ataxia, Pendred syndrome, Distal spinal muscular atrophy type 1, Multicentric carpotarsal osteolysis syndrome, Methemoglobinemia, Hereditary spastic paraplegia, Alport syndrome, Pelizaeus–Merzbacher disease, Distal renal tubular acidosis, Rhizomelic chondrodysplasia punctata, Hypogammaglobulinemia, Hereditary sensory and autonomic neuropathy, Microcephaly, Ectrodactyly, Klippel–Feil syndrome, Optic neuropathy, Aplasia cutis congenita, Charcot–Marie–Tooth disease, Aarskog–Scott syndrome, Benign infantile epilepsy, Nephrogenic diabetes insipidus, Kinky hair, Multicystic dysplastic kidney, Congenital nephrotic syndrome, Hair loss, Benign familial neonatal seizures, Hydrocephalus, Dandy–Walker malformation, Hay–Wells syndrome, B Positive, Richard_J._Berry, 上峰町, Симфонія_№_37_(Моцарт), بيت_أبو_مرعى_(أرحب), Tikus_Desa_dan_Tikus_Kota, Нападение_в_джунглях, The_Miraculous_Draught_of_Fishes_(Jordaens), Mi_wonton, Istana_Stockholm, Kimberley_Echo, ショーン・チャコーン, Judo, Dodge_50_Series, SMA_Negeri_8_Medan, Кабрал_ди_Мелу_Нету,_Жуан, Currys_Digital, George_I_of_Great_Britain, Rumah_tradisional_Perak, Swing_Kids_(2018_film), شابة_وجميلة_(فيلم), Райс,_Энгаури, تنفس_بطني, Margaret_(film), Bantarkawung,_Brebes, help:referencing_for_beginners, Limón_de_San_Lucas_del_Maíz, Dance_Evolution, Giampaolo_Pansa, Предсказание_структуры_белка, Say_Something_(A_Great_Big_World_song), Living_(2012_film), Ab_Khvor, 2014_MLS_All-Star_Game, Johann_Gottfried_Herder, Ralph_Belknap_Baldwin, Nuria_Ibáñez, List_of_acts_of_the_Parliament_of_the_United_Kingdom,_1930–1938, Hizbullah_(Indonesia), فيزياء_حيوية, Залізна_сотня, Metro-Goldwyn-Mayer, The_Drowning_(film), 1784_in_Canada, 1_Samuel_18, Poet_laureate, Funny_Face_(musical), Шерман_(округ,_Техас), Keuskupan_Jackson, Kembang_bangkai, Socratea_exorrhiza, Давид_XI, أوك_تايك_يون, 500_Series_Shinkansen, Shuang_Xing, Dimitrie_Gusti, بوابة:كمال_الأجسام, Серебряный_рубль, Fromberg,_Montana, 1872_United_States_House_of_Representatives_election_in_Florida, Ari_Prasetya, Maureen_Ogden, The_Day_a_Pig_Fell_into_the_Well, Papirus_49, John_Tembo, Emmitt_Smith, シーキングザダイヤ, Lambang_Persemakmuran_Polandia-Lituania, Shane_Larkin, 5th_Conference_of_the_International_Woman_Suffrage_Alliance, الغواصة_الألمانية_يو-106_(1940), Simón_Arboleda, 中村正三郎_(政治家), John_Boccieri, Историја_Србије_у_старом_веку, قضية_نيجريرا, Dieci_piccoli_indiani