Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Breast milk stool (finding) | 249621006 | |
| Total ossicular replacement prosthesis (physical object) | 257339006 | |
| CA 125 measurement (procedure) | 80529009 | |
| Entire phalanx of index finger (body structure) | 361783009 | |
| Allergy to pyrimethamine (finding) | 294388006 | |
| Entire fetal cranial vault (body structure) | 155641002 | |
| Aneurysm of right ventricle following procedure (disorder) | 880044007 | |
| Odor of urine (observable entity) | 364688007 | |
| Mitochondrial respiratory chain complex I structural subunit gene defect (disorder) | 1196872006 | |
| Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type (disorder) | 725407006 | [A subtype of dystrophic epidermolysis bullosa characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities.The disease manifests at birth or during the neonatal period with generalized blistering. Aplasia cutis congenita can also be observed at birth. The disease is caused by mutations within the type VII collagen gene (COL7A1) that lead to an alteration of function or a reduction in the amounts of collagen VII. This impairs collagen VII assembly into anchoring fibrils which anchor the basement membrane to the underlying dermis. This in turn causes reduced skin resistance to minor trauma. Transmission is autosomal recessive., A subtype of dystrophic epidermolysis bullosa characterised by generalised cutaneous and mucosal blistering that is not associated with severe deformities.The disease manifests at birth or during the neonatal period with generalised blistering. Aplasia cutis congenita can also be observed at birth. The disease is caused by mutations within the type VII collagen gene (COL7A1) that lead to an alteration of function or a reduction in the amounts of collagen VII. This impairs collagen VII assembly into anchoring fibrils which anchor the basement membrane to the underlying dermis. This in turn causes reduced skin resistance to minor trauma. Transmission is autosomal recessive.] |
| Circulating fluid whole body heating/cooling pad system (physical object) | 711594001 | |
| Entire greater femoral trochanter subregion of hip region (body structure) | 731485003 | |
| Entire third dorsal interosseous of hand (body structure) | 245005009 | |
| Structure of third dorsal interosseous muscle of hand (body structure) | 1179651001 | |
| Infant feeding problem (finding) | 161838002 | |
| Powered rectal irrigation system control unit (physical object) | 704947006 | |
| Structure of superficial posterior crural muscle (body structure) | 1172381001 | |
| Entire hypoglossal nerve (body structure) | 362471008 | |
| Tumor invasion by direct extension from organ of origin to adjacent organ (finding) | 409771002 | |
| Adiposogenital dystrophy (disorder) | 62999006 |