Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Embolization of vascular device fragment during cardiac catheterization (disorder) | 473163005 | |
| Septal defect prosthesis (physical object) | 360230006 | |
| Wheelchair, occupant-driven, bimanual-lever-operated, non-collapsible (physical object) | 466229005 | |
| Virus isolated but not further identified (finding) | 446613002 | |
| Removal of skull plate (procedure) | 17669008 | |
| Malignant melanoma of skin of left wrist (disorder) | 985355341000119101 | |
| Disappearing bone disease (disorder) | 240161003 | |
| Pressure injury of right heel stage IV (disorder) | 29881000175107 | |
| Excision of fascia of posterior abdominal wall (procedure) | 178043001 | |
| Skin color good (finding) | 304228008 | |
| Electrical transformer fitter (occupation) | 11125006 | |
| Autosomal recessive progressive external ophthalmoplegia (disorder) | 827117008 | [A rare genetic neuro-ophthalmological disease with characteristics of progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse, symmetric ophthalmoparesis. Additional signs may include generalized skeletal muscle weakness, muscle atrophy, sensory axonal neuropathy, ataxia, cardiomyopathy, and psychiatric symptoms. It is usually more severe than autosomal dominant form., A rare genetic neuro-ophthalmological disease with characteristics of progressive weakness of the external eye muscles, resulting in bilateral ptosis and diffuse, symmetric ophthalmoparesis. Additional signs may include generalised skeletal muscle weakness, muscle atrophy, sensory axonal neuropathy, ataxia, cardiomyopathy, and psychiatric symptoms. It is usually more severe than autosomal dominant form.] |
| Entire fourth dorsal interosseous of hand (body structure) | 245006005 | |
| Ability to self-administer parenteral medication (observable entity) | 404983006 | |
| All bone marrow of humerus (body structure) | 731604008 | |
| Liquid stool specimen (specimen) | 16223531000119100 | |
| X-linked dystonia parkinsonism (disorder) | 698279003 | |
| Entire medial sural cutaneous nerve (body structure) | 215828004 | |
| Uterine cervix endoscopy (procedure) | 120042008 | |
| Lack of posterior occlusal support (finding) | 312401000119103 |