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diccionario analógico

monogenic disease, monogenic disorder - polygenic disease, polygenic disorder - achondroplasia, achondroplasty, chondrodystrophy, osteosclerosis congenita軟骨形成不全, 軟骨発育不全 - abetalipoproteinemia無βリポタンパク質血症 - inborn error of metabolism - aganglionic megacolon, congenital megacolon, Hirschsprung's disease, Hirschsprung disease, pelvirectal achalasia - mucopolysaccharidosis - hyperbetalipoproteinemia - ichthyosis魚鱗癬 - branched chain ketoaciduria, maple syrup urine disease楓糖尿症 - McArdle's disease - dystrophy, muscular dystrophyきんいしゅくしょう, きんジストロフィー, ジストロフィー, 筋ジストロフィー, 筋委縮症, 筋萎縮症 - oligodactyly - oligodontia - otosclerosis - autosomal dominant disease, autosomal dominant disorder - autosomal recessive defect, autosomal recessive disease - aplastic anemia with congenital anomalies, aplastic infantile funicular myelosis, congenital aplastic anemia, congenital hypoplastic anemia, congenital pancytopenia, constitutional infantile panmyelopathy, familial aplastic anemia with multiple congenital defects, familial constitutional panmyelopathy, familial hypoplastic anemia, Fanconi's anaemia, Fanconi's anemia, Fanconi's pancytopenia, Fanconi's panmyelopathy, Fanconi's refractory anemia - juvenile amaurotic idiocy, Spielmeyer-Vogt disease - congenital afibrinogenemia - Albers-Schonberg disease, marble bones disease, osteopetrosis大理石骨病 - nevoid elephantiasis, pachyderma強皮症 - dwarfism, nanism小人症 - lactase deficiency, lactose intolerance, milk intolerance乳糖不耐症 - porphyriaポルフィリン症 - hepatolenticular degeneration, Wilson's disease肝レンズ核変性症[Spéc.]

congenital disease (n.) • genetic abnormality (n.) • genetic defect (n.) • genetic disease (n.) • genetic disorder (n.) • hereditary condition (n.) • hereditary disease (n.) • inherited disease (n.) • inherited disorder (n.) • 遺伝子疾患 (n.) • 遺伝病 (n.)

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