Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Ex-smoker for less than 1 year (finding) | 735128000 | |
| Skeletal survey - pediatric - trauma (procedure) | 241099002 | |
| Removal of valve of vas deferens (procedure) | 59230000 | |
| Periostitis without osteomyelitis of thoracic spine (disorder) | 203257002 | |
| Repair of perineal tear (procedure) | 237026005 | |
| Oita 293 virus (organism) | 65678003 | |
| Spinal fusion for kyphosis (procedure) | 429769008 | |
| Loxosceles rufescens (organism) | 72418007 | |
| Ulcer of tunica vaginalis (disorder) | 18682003 | |
| Amyloid of ureter (disorder) | 282357008 | |
| Salmonella Ilugun (organism) | 63015008 | |
| Coleslaw with reduced calorie dressing (substance) | 227934007 | |
| Sebaceous cyst of left eyelid (disorder) | 15732121000119106 | |
| Cefsulodin adverse reaction (disorder) | 293015000 | |
| Product containing precisely erythromycin (as erythromycin stearate) 500 milligram/1 each conventional release oral tablet (clinical drug) | 324181004 | |
| Entire mucocutaneous junction of lip (body structure) | 727267009 | |
| Apgar at 10 minutes = 5 (finding) | 169928006 | |
| Focal cortical dysplasia type IIa (disorder) | 1003429001 | [Focal cortical dysplasia is a congenital abnormality with abnormal organization of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type II usually presents in children. More extensive changes occur outside the temporal lobe and commonly in the frontal lobe. Type IIa is histologically distinct due to the absence of balloon cells., Focal cortical dysplasia is a congenital abnormality with abnormal organisation of the cortical layers of the brain. These lesions frequently cause refractory epilepsy. Type II usually presents in children. More extensive changes occur outside the temporal lobe and commonly in the frontal lobe. Type IIa is histologically distinct due to the absence of balloon cells.] |
| Pre-eruptive intracoronal resorption of tooth (disorder) | 700238000 | |
| M line (cell structure) | 27112006 |