Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Office of Population Census and Surveys hearing disability scale score (observable entity) | 717033008 | |
| Biopsy of bilateral kidneys using fluoroscopic guidance (procedure) | 19531000087109 | |
| Injection into tendon of elbow (procedure) | 787796004 | |
| Tompkins metroplasty (procedure) | 236905004 | |
| Product containing precisely clozapine 50 milligram/1 milliliter conventional release oral suspension (clinical drug) | 1163332008 | |
| Sphoeroides annulatus (organism) | 55943002 | |
| Platacanthomys lasiurus (organism) | 395462001 | |
| Genus Platacanthomys (organism) | 395461008 | |
| Musculoskeletal structure of finger of left hand (body structure) | 898145008 | |
| Minimal deviation adenocarcinoma of endocervical type (morphologic abnormality) | 388986005 | |
| Specimen from parathyroid obtained by fine needle aspiration biopsy (specimen) | 432141003 | |
| Parathyroid biopsy specimen (specimen) | 309151003 | |
| Anesthesia for thoracotomy procedure involving mediastinum (procedure) | 54547003 | |
| Replacement of cardiac biventricular permanent pacemaker using fluoroscopic guidance (procedure) | 448869001 | |
| Eliciting a speech response (regime/therapy) | 311585002 | |
| Closed lateral dislocation of proximal end of tibia (disorder) | 9787009 | |
| History of proteinuria (situation) | 473110002 | |
| Keutel syndrome (disorder) | 724208006 | [Syndrome with characteristics of diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism. The abnormal calcification principally involves the cartilage of the ears, nose, larynx and the tracheobronchial tree. Epiphyseal stippling of the long bones and calcification of the spinal column vertebrae have also been reported. The dysmorphism is characterized by an elongated face with maxillary and midface hypoplasia. Other associated features may include hearing loss and recurrent otitis and/or sinusitis, mild intellectual deficit, frequent respiratory infections, nasal speech and, more rarely, seizures and short stature. The syndrome is caused by mutations in the gene encoding the matrix Gla protein (MGP, located at 12p13.1-p12.3). The syndrome is transmitted as an autosomal recessive trait., Syndrome with characteristics of diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism. The abnormal calcification principally involves the cartilage of the ears, nose, larynx and the tracheobronchial tree. Epiphyseal stippling of the long bones and calcification of the spinal column vertebrae have also been reported. The dysmorphism is characterised by an elongated face with maxillary and midface hypoplasia. Other associated features may include hearing loss and recurrent otitis and/or sinusitis, mild intellectual deficit, frequent respiratory infections, nasal speech and, more rarely, seizures and short stature. The syndrome is caused by mutations in the gene encoding the matrix Gla protein (MGP, located at 12p13.1-p12.3). The syndrome is transmitted as an autosomal recessive trait.] |
| Bronze color (qualifier value) | 371258006 | |
| Complete excision of lung with mediastinal dissection (procedure) | 91596000 |