Carrier of disorder (finding)
| Code | 29679002 |
|---|---|
| Semantic tag | finding |
| Module | international |
| Definition | primitive |
| Effective time | 20020131 |
404684003Clinical finding
finding
846991000000100Carrier of Connexin 26 gene mutation
finding
758911000000107Carrier of Duchenne muscular dystrophy gene mutation
finding
441646007Carrier of Tay Sachs disease gene mutation
finding
928371000000109Carrier of VLCAD (very long chain acyl-coenzyme A dehydrogenase deficiency) gene mutation
finding
1052091000000103Carrier of X-linked Alport syndrome COL4A5 (collagen type IV alpha 5) gene mutation
finding
1052101000000106Carrier of autosomal Alport syndrome COL4A3 (collagen type IV alpha 3) gene mutation
finding
1052111000000108Carrier of autosomal Alport syndrome COL4A4 (collagen type IV alpha 4) gene mutation
finding
66611000119101Carrier of chromosome disorder
finding
441520002Carrier of cystic fibrosis gene mutation
finding
811761000000109Carrier of fragile X gene mutation
finding
736703007Carrier of haemochromatosis HFE gene mutation
finding
66598005Carrier of infectious organism
finding
822891000000105Carrier of medium chain acyl-coenzyme A dehydrogenase deficiency gene mutation
finding
66871000119108Carrier of metabolic disorder
finding
286471000119100Carrier of neurogenetic disorder
finding
442018007Carrier of sickle cell gene mutation
finding
87955000Carrier state, disease expressed
finding
24800002Carrier state, disease not expressed
finding
47461006Genetic disorder carrier
finding
191301000Haemophilia carrier
finding
302801000000107Non-significant carrier of disorder
finding
946701000000104Phenylketonuria gene carrier
finding
302811000000109Significant carrier of disorder
finding