Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Carbophilus carboxidus (organism) | 434054009 | |
| Construction of temporary dental bridge (procedure) | 281236004 | |
| No undue priority given to drink-related activities (situation) | 228333007 | |
| Drinking habits (observable entity) | 228282009 | |
| Renal sclerosis with hypertension (disorder) | 14973001 | |
| Manual removal of retained placenta (procedure) | 28233006 | |
| Product containing piroxicam in parenteral dose form (medicinal product form) | 437905005 | |
| Product containing precisely choriogonadotropin alfa 500 microgram/1 milliliter conventional release solution for injection (clinical drug) | 781804006 | |
| Product containing precisely pitolisant (as pitolisant hydrochloride) 4.45 milligram/1 each conventional release oral tablet (clinical drug) | 1156170005 | |
| Entire distal epiphysis of ulna (body structure) | 302521000 | |
| Left lower lobe bronchus cytologic material (specimen) | 110923006 | |
| Physiological mobilization of the temporomandibular joint (regime/therapy) | 229429008 | |
| Balloon dilatation of right ventricular outflow tract (procedure) | 233067004 | |
| Unable to comply with treatment (finding) | 372089002 | |
| Product containing droxidopa (medicinal product) | 426457000 | |
| Abrasion of skin of left shoulder region (disorder) | 11823601000119100 | |
| Aneurysm of pararenal aorta (disorder) | 871536000 | |
| 15.885 (qualifier value) | 732514005 | |
| Ultrasound great vessel scan (procedure) | 169243002 | |
| 15q overgrowth syndrome (disorder) | 771477003 | [A rare partial autosomal trisomy/tetrasomy characterised by facial dysmorphism (long thin face, prominent forehead, down-slanting palpebral fissures, prominent nose with broad nasal bridge, prominent chin), pre and postnatal overgrowth, renal anomalies (for example horseshoe kidney, renal agenesis, hydronephrosis), mild to severe learning difficulties and behavioural abnormalities. Additional features may include craniosynostosis and macrocephaly., A rare partial autosomal trisomy/tetrasomy characterized by facial dysmorphism (long thin face, prominent forehead, down-slanting palpebral fissures, prominent nose with broad nasal bridge, prominent chin), pre and postnatal overgrowth, renal anomalies (for example horseshoe kidney, renal agenesis, hydronephrosis), mild to severe learning difficulties and behavioral abnormalities. Additional features may include craniosynostosis and macrocephaly.] |