Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Abscess of Rutherford Morison pouch (disorder) | 235995003 | |
| Inanimate samples and substances (navigational concept) | 258619000 | |
| Metastatic malignant neoplasm to glomus jugulare (disorder) | 94316002 | |
| Fluoroscopic arthrography of ankle joint with contrast (procedure) | 430308003 | |
| Ankle joint laxity (finding) | 298217004 | |
| Lardy cake (substance) | 226659009 | |
| Centers for Disease Control and Prevention Class III/Contaminated (finding) | 419877002 | |
| Baby overdue (finding) | 249122000 | |
| Revision of exenteration of eye cavity with secondary graft (procedure) | 14265004 | |
| Cladotanytarsus lewisi specific immunoglobulin E (substance) | 388408003 | |
| Objective observation (qualifier value) | 260224007 | |
| Excessive beta glucan intake (finding) | 440481000124106 | [Higher intake of beta glucan compared to established reference standards or recommendations based on physiological needs.] |
| Mental health functional therapies - 24 hr not intensive (procedure) | 391253008 | |
| Product containing precisely artesunate 60 milligram/1 vial powder for conventional release solution for injection (clinical drug) | 1197390008 | |
| Goldmann-Favre syndrome (disorder) | 232065000 | [A vitreoretinal dystrophy with characteristics of early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular oedema, retinoschisis). The onset is usually in childhood. Mutations in the NR2E3 gene (formerly called PNR) have been identified in some patients. NR2E3 (15q23) encodes a retinal nuclear receptor that is involved in the differentiation of photoreceptors. Inherited as an autosomal recessive trait and has a progressive course., A vitreoretinal dystrophy with characteristics of early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis). The onset is usually in childhood. Mutations in the NR2E3 gene (formerly called PNR) have been identified in some patients. NR2E3 (15q23) encodes a retinal nuclear receptor that is involved in the differentiation of photoreceptors. Inherited as an autosomal recessive trait and has a progressive course.] |
| Postimmersion-submersion syndrome (disorder) | 89687005 | |
| Non-cardiogenic pulmonary edema (disorder) | 95437004 | |
| Structure of superior corneal limbus of right eye (body structure) | 840710008 | |
| Mycoplasma opalescens (organism) | 66157008 | |
| Low food antioxidant diet (finding) | 226184006 |