Engelsk navneord: monogenic disease |
| 1. | monogenic disease (om tilstand) an inherited disease controlled by a single pair of genes |
|
| Termer med samme betydning (synonymer) | monogenic disorder |
|
| Mindre specifikke termer | congenital disease, genetic abnormality, genetic defect, genetic disease, genetic disorder, hereditary condition, hereditary disease, inherited disease, inherited disorder |
|
| Mere specifikke termer | CF, crescent-cell anaemia, crescent-cell anemia, cystic fibrosis, drepanocytic anaemia, drepanocytic anemia, dysostosis multiplex, familial hypercholesterolemia, fibrocystic disease of the pancreas, gargoylism, Gaucher's disease, Huntington's chorea, Huntington's disease, Hurler's disease, Hurler's syndrome, infantile amaurotic idiocy, lipochondrodystrophy, Mediterranean anaemia, Mediterranean anemia, mucoviscidosis, neurofibromatosis, pancreatic fibrosis, Sachs disease, SCID, severe combined immunodeficiency, severe combined immunodeficiency disease, sickle-cell anaemia, sickle-cell anemia, sickle-cell disease, Tay-Sachs, Tay-Sachs disease, thalassaemia, thalassemia, von Recklinghausen's disease |
|
