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disease, sickness — 病, 病症, 症[Hyper.]
monogenic disease, monogenic disorder — 遗传病 - polygenic disease, polygenic disorder — 多基因遗传证 - achondroplasia, achondroplasty, chondrodystrophy, osteosclerosis congenita — 软骨发育不全 - abetalipoproteinemia — 血症 - inborn error of metabolism - aganglionic megacolon, congenital megacolon, Hirschsprung's disease, Hirschsprung disease, pelvirectal achalasia - mucopolysaccharidosis — 粘多糖病 - hyperbetalipoproteinemia - ichthyosis — 干皮病, 鱼鳞病, 鳞癣 - branched chain ketoaciduria, maple syrup urine disease — 枫糖尿症 - McArdle's disease — 麦卡德尔病 - dystrophy, muscular dystrophy — 肌肉萎缩症, 营养失调 - oligodactyly — 少指 - oligodontia — 少牙 - otosclerosis — 耳硬化症 - autosomal dominant disease, autosomal dominant disorder — 显性遗传病 - autosomal recessive defect, autosomal recessive disease — 隐形遗传病 - 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 — 范康尼贫血 - juvenile amaurotic idiocy, Spielmeyer-Vogt disease - congenital afibrinogenemia - Albers-Schonberg disease, marble bones disease, osteopetrosis — 骨石化病 - nevoid elephantiasis, pachyderma — 皮肤肥厚 - dwarfism, nanism — 侏儒症 - lactase deficiency, lactose intolerance, milk intolerance — 乳糖不耐症 - porphyria — 卟啉症, 紫质症 - hepatolenticular degeneration, Wilson's disease — 威尔森氏症, 肌震颤性综合征, 肝豆状核变性[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.) • 遗传病 (n.)