Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Intracardiac oximeter (physical object) | 469525004 | |
| Draining sinus co-occurrent and due to chronic osteomyelitis of ankle (disorder) | 295831000119109 | |
| Entire peroneal compartment of lower leg (body structure) | 264145004 | |
| Hemodialysis technique (qualifier value) | 446402005 | |
| Ecthyma caused by Streptococcus pyogenes (disorder) | 762693003 | |
| Debridement of open fracture of metacarpal bone (procedure) | 448933005 | |
| Effusion of olecranon bursa of bilateral elbows (disorder) | 15725281000119106 | |
| Entire manubriosternal joint (body structure) | 263312002 | |
| Product containing precisely ceritinib 150 milligram/1 each conventional release oral tablet (clinical drug) | 1003497006 | |
| Aquaporin-4 antibody (substance) | 445426002 | |
| Bajan (qualifier value) | 262336008 | |
| Microscopic examination of specimen from periureteral tissue for parasites (procedure) | 608900009 | |
| Tongueworm cyst (disorder) | 240911006 | |
| Immunodeficiency due to ficolin 3 deficiency (disorder) | 766705006 | [A rare genetic immunodeficiency due to a complement cascade protein anomaly characterised by low or undetectable serum ficolin 3 levels, susceptibility to infections and possibly autoimmunity. The presentation is variable, from perinatal necrotising enterocolitis and recurrent skin infections with Staphylococcus aureus to childhood-onset recurrent pulmonary infections leading to brain abscesses and pulmonary fibrosis, to membranous nephropathy. In some patients clinical consequences of ficolin 3 deficiency were not clear. There is evidence that ficolin 3 deficiency is caused by homozygous mutation in the FCN3 gene on chromosome 1p36., A rare genetic immunodeficiency due to a complement cascade protein anomaly characterized by low or undetectable serum ficolin 3 levels, susceptibility to infections and possibly autoimmunity. The presentation is variable, from perinatal necrotizing enterocolitis and recurrent skin infections with Staphylococcus aureus to childhood-onset recurrent pulmonary infections leading to brain abscesses and pulmonary fibrosis, to membranous nephropathy. In some patients clinical consequences of ficolin 3 deficiency were not clear. There is evidence that ficolin 3 deficiency is caused by homozygous mutation in the FCN3 gene on chromosome 1p36.] |
| Entire cricothyroid branch of superior thyroid artery (body structure) | 160495002 | |
| Local anesthetic infiltration of upper lid (procedure) | 231339005 | |
| Accessory tissue on left atrioventricular valve leaflet (disorder) | 253499008 | |
| Entire lingual surface of tooth (body structure) | 362104007 | |
| Ability to move jaw repeatedly (observable entity) | 285447001 | |
| Egophony (finding) | 19977002 |