All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Examination for alleged rape (procedure) | 171403008 | |
| History of dysplasia of prostate (situation) | 10988211000119104 | |
| Telepractice consultation (procedure) | 763184009 | |
| Large intestine, proximal surgical margin, involved by tumor (finding) | 369690005 | |
| Order Amphisphaeriales (organism) | 765241004 | |
| Lipodystrophy caused by antiretroviral drug (disorder) | 713693008 | |
| Hide flesher and dehairer (hand) (occupation) | 72733000 | |
| Mucopurulent sputum (finding) | 8955008 | |
| Down's screening - blood sent (finding) | 169797001 | |
| Onychocytic matricoma (disorder) | 773641008 | [A rare benign nail tumor originating in the nail matrix characterized by localized pachyonychia and variable degrees of pigmentation: pigmented, melanocytic (common, longitudinal melanonychia that may simulate a foreign body) or hypopigmented. Histopathology demonstrates a purely epithelial tumor with endo-keratinization in the deep portion and concentrically arranged nests of pre-keratogenous and keratogenous cells., A rare benign nail tumour originating in the nail matrix characterised by localised pachyonychia and variable degrees of pigmentation: pigmented, melanocytic (common, longitudinal melanonychia that may simulate a foreign body) or hypopigmented. Histopathology demonstrates a purely epithelial tumour with endo-keratinisation in the deep portion and concentrically arranged nests of pre-keratogenous and keratogenous cells.] |
| Boggy prostate (finding) | 431469000 | |
| Atriplex lentiformis specific diagnostic allergen extract (product) | 411947006 | |
| Verbalizes prescribed activity plan (finding) | 417938007 | |
| Haim Munk syndrome (disorder) | 719973009 | [A rare syndrome with characteristics of palmoplantar hyperkeratosis, severe early-onset periodontitis, onychogryposis, pes planus, arachnodactyly and acroosteolysis. The syndrome presents with severe and extensive skin manifestations. Severe, early-onset progressive periodontitis that affects both the deciduous and permanent dentitions and presents with gingival inflammation and alveolar bone destruction is a hallmark of the disease. Onychogryposis, arachnodactyly, acroosteolysis and pes planus are additional features that help to distinguish from other forms of palmoplantar hyperkeratosis. The syndrome is caused by germline mutations in the lysosomal protease cathepsin C (CTSC) gene mapped to chromosome 11q14.1-q14.3. It is transmitted as an autosomal recessive trait.] |
| Postmortem radiographic imaging of whole body (procedure) | 169112002 | |
| Doppler ultrasonography of arteries of bilateral upper limbs (procedure) | 6761000087104 | |
| Lymphangioma of orbit (disorder) | 414626005 | |
| Increased cortisone level (finding) | 131083006 | |
| Accident caused by explosion of methane (event) | 218113001 | |
| Orthodontic bracket adhesive (physical object) | 464142004 |