| 释义 | monogenic disorderThesaurus
 EncyclopediaSeedisorder| Noun | 1. |  monogenic disorder - an inherited disease controlled by a single pair of genesmonogenic diseaseSCID, severe combined immunodeficiency, severe combined immunodeficiency disease - a congenital disease affecting T cells that can result from a mutation in any one of several different genes; children with it are susceptible to infectious disease; if untreated it is lethal within the first year or two of lifecongenital disease, genetic abnormality, genetic defect, genetic disease, genetic disorder, hereditary condition, hereditary disease, inherited disease, inherited disorder - a disease or disorder that is inherited geneticallycystic fibrosis, fibrocystic disease of the pancreas, mucoviscidosis, pancreatic fibrosis, CF - the most common congenital disease; the child's lungs and intestines and pancreas become clogged with thick mucus; caused by defect in a single gene; no cure is knownGaucher's disease - a rare chronic disorder of lipid metabolism of genetic originHuntington's chorea, Huntington's disease - hereditary disease; develops in adulthood and ends in dementiadysostosis multiplex, gargoylism, Hurler's disease, Hurler's syndrome, lipochondrodystrophy - hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardationneurofibromatosis, von Recklinghausen's disease - autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalitiescrescent-cell anaemia, crescent-cell anemia, drepanocytic anaemia, drepanocytic anemia, sickle-cell anaemia, sickle-cell anemia, sickle-cell disease - a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shapeinfantile amaurotic idiocy, Sachs disease, Tay-Sachs, Tay-Sachs disease - a hereditary disorder of lipid metabolism occurring most frequently in individuals of Jewish descent in eastern Europe; accumulation of lipids in nervous tissue results in death in early childhoodMediterranean anaemia, Mediterranean anemia, thalassaemia, thalassemia - an inherited form of anemia caused by faulty synthesis of hemoglobinfamilial hypercholesterolemia - congenital disorder characterized by high levels of cholesterol and early development of atherosclerosis | 
 monogenic disorder
 monogenic disorderA disorder caused by mutation of a single gene—i.e., based on simple mendelian genetics.monogenic disorder
 Synonyms for monogenic disordernoun an inherited disease controlled by a single pair of genesSynonymsRelated WordsSCIDsevere combined immunodeficiencysevere combined immunodeficiency diseasecongenital diseasegenetic abnormalitygenetic defectgenetic diseasegenetic disorderhereditary conditionhereditary diseaseinherited diseaseinherited disordercystic fibrosisfibrocystic disease of the pancreasmucoviscidosispancreatic fibrosisCFGaucher's diseaseHuntington's choreaHuntington's diseasedysostosis multiplexgargoylismHurler's diseaseHurler's syndromelipochondrodystrophyneurofibromatosisvon Recklinghausen's diseasecrescent-cell anaemiacrescent-cell anemiadrepanocytic anaemiadrepanocytic anemiasickle-cell anaemiasickle-cell anemiasickle-cell diseaseinfantile amaurotic idiocySachs diseaseTay-SachsTay-Sachs diseaseMediterranean anaemiaMediterranean anemiathalassaemiathalassemiafamilial hypercholesterolemia
 |