Engelsk navneord: genetic defect |
| 1. | genetic defect (om tilstand) a disease or disorder that is inherited genetically |
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| Termer med samme betydning (synonymer) | congenital disease, genetic abnormality, genetic disease, genetic disorder, hereditary condition, hereditary disease, inherited disease, inherited disorder |
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| Mindre specifikke termer | disease |
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| Mere specifikke termer | abetalipoproteinemia, achondroplasia, achondroplasty, Albers-Schonberg disease, autosomal dominant disease, autosomal dominant disorder, autosomal recessive defect, autosomal recessive disease, branched chain ketoaciduria, chondrodystrophy, congenital afibrinogenemia, congenital megacolon, congenital pancytopenia, dwarfism, dystrophy, Fanconi's anaemia, Fanconi's anemia, hepatolenticular degeneration, Hirschsprung's disease, hyperbetalipoproteinemia, ichthyosis, inborn error of metabolism, juvenile amaurotic idiocy, lactase deficiency, lactose intolerance, maple syrup urine disease, marble bones disease, McArdle's disease, milk intolerance, monogenic disease, monogenic disorder, mucopolysaccharidosis, muscular dystrophy, nanism, nevoid elephantiasis, oligodactyly, oligodontia, osteopetrosis, osteosclerosis congenita, otosclerosis, pachyderma, polygenic disease, polygenic disorder, porphyria, Spielmeyer-Vogt disease, Wilson's disease |
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