Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Biacuplasty of intervertebral disc using fluoroscopic guidance (procedure) | 1148824000 | |
| Product containing only acetone (medicinal product) | 774421004 | |
| Lymphocyte positive for CD73 antigen (cell) | 117407000 | |
| Pin-sleeve orthopedic bone screw (physical object) | 701701009 | |
| Multiple epiphyseal dysplasia type 4 (disorder) | 715672007 | [A multiple epiphyseal dysplasia with a late-childhood onset manifesting as joint pain involving hips, knees, wrists and fingers with occasional limitation of joint movements, deformity of hands, feet, and knees, scoliosis and slightly reduced adult height. Follows an autosomal recessive mode of transmission] |
| Sepsis caused by Proteus (disorder) | 1149486001 | |
| Post-chemotherapy testicular hypofunction (disorder) | 236813004 | |
| Helium gas cylinder F (physical object) | 337546007 | |
| Jaeger type 12 (finding) | 260250006 | |
| Family history of problem behavior (situation) | 430334006 | |
| Rubella vaccination contraindicated (situation) | 719473004 | |
| Radiofrequency rhizotomy of trigeminal nerve (procedure) | 736132002 | |
| Laparoscopic cholecystostomy (procedure) | 450500003 | |
| Admission by rehabilitation physician (procedure) | 305283008 | |
| Increased muscle tone - right side more than left side (finding) | 424676008 | |
| Gastrojejunal junction (morphologic abnormality) | 264051006 | |
| Family history unknown (situation) | 407559004 | |
| Maturity-onset diabetes of the young, type 8 (disorder) | 609575003 | |
| Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) | 763775000 | [An inherited epidermal disorder with characteristics of palmoplantar keratoderma, linear hyperkeratotic papules on the flexural side of large joints (cord-like distribution around wrists, in antecubital and popliteal folds), hyperkeratotic plaques (on neck, axillae, elbows, wrists, and knees), mild ichthyosiform scaling, and sclerotic constrictions around fingers that present flexural deformities. The disease is caused by homozygous mutation in the POMP gene.] |
| Aspergillus nomius (organism) | 10101000087100 |