Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Diplectrum formosum (organism) | 59838003 | |
| Crotalaria juncea (organism) | 5525009 | |
| Occlusion of superior mesenteric artery (disorder) | 427592000 | |
| Arachidonic acid requirement (observable entity) | 226263008 | |
| Omega 6 fatty acid requirement (observable entity) | 226264002 | |
| Subsequent nursing facility visit (procedure) | 18170008 | |
| Two plane mold (physical object) | 228755002 | |
| Myxotrichum deflexum (organism) | 214517781000087109 | |
| Glossina palpalis (organism) | 72576000 | |
| Datura candida (organism) | 40142004 | |
| Estimated quantity of intake of psyllium in 24 hours (observable entity) | 896798006 | [The approximate quantity of intake in one day of psyllium.] |
| Lipoma of lower leg (disorder) | 189004003 | |
| Human alphaherpesvirus 3 clade 4 (organism) | 725472004 | |
| 2q32q33 microdeletion syndrome (disorder) | 719659003 | [A recently described syndrome with characteristics of a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features. It has been described in fewer than 25 patients to date. Facial features include downslanting palpebral fissures, low-set ears and prominent nasal bridge. Most patients also have a high-arched palate or cleft palate. Some individuals have an ectodermal dysplasia-like phenotype, with thin, transparent skin and abnormalities of the hair and teeth. The size of the deletions is variable from 35 kb to 10.4 Mb. Haploinsufficiency of SATB2 is responsible for several of the clinical features.] |
| 8q12 microduplication syndrome (disorder) | 719684000 | [Syndrome associated with unusual and characteristic multi-organ clinical features, which include hearing loss, congenital heart defects, intellectual disability, hypotonia in infancy and Duane anomaly. It has been described in two patients. The lack of recurrent breakpoints in these two cases and the absence of any low-copy repeats pairs that flank these de novo events do not support non-allelic homologous recombination as the mutation mechanism. The 8q12 region includes CHD7 and it is proposed that this gene, associated with CHARGE syndrome by haploinsufficiency, causes a different phenotype by gain-of-dosage.] |
| GP1c-ganglioside (substance) | 117721002 | |
| Product containing only gatifloxacin in parenteral dose form (medicinal product form) | 779357008 | |
| Intermittent Bence Jones proteinuria (finding) | 1144918001 | |
| Reconstruction of common iliac artery (procedure) | 233345007 | |
| Reconstruction of iliac artery (procedure) | 265516003 |