Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Ethyl phosphate (substance) | 84987009 | |
| Blood group antigen Alda (substance) | 69373009 | |
| Midproliferative endometrium (morphologic abnormality) | 448736007 | |
| Familial dementia Danish type (disorder) | 783258000 | [A rare neurodegenerative disease with characteristics of progressive cataracts, hearing loss, cerebellar ataxia, paranoid psychosis and dementia. Neuropathological features are diffuse atrophy of all parts of the brain, chronic diffuse encephalopathy and the presence of extremely thin and almost completely demyelinated cranial nerves. Caused by mutation in the ITM2B gene.] |
| Product containing colchicine in oral dose form (medicinal product form) | 768266001 | |
| History of fibromatosis (situation) | 59591000119105 | |
| Trichodiene synthase (substance) | 130829003 | |
| Substance with 3',5'-cyclic-nucleotide phosphodiesterase inhibitor mechanism of action (substance) | 782490003 | |
| Drilling-machine setter-operator (occupation) | 79266003 | |
| Spouse works away from home (situation) | 161075006 | |
| Free aldosterone (substance) | 706950007 | |
| Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency (disorder) | 34194007 | |
| Histologic type of primary malignant neoplasm of colon (observable entity) | 798721000004104 | |
| Coproporphyrin 2 isomer (substance) | 406514002 | |
| Deficiency of adenylate kinase (disorder) | 124340003 | |
| Structure of accessory nerve spinal portion (body structure) | 52658004 | |
| Housing estate (environment) | 224809004 | |
| Lymphocyte antigen CDw75 (substance) | 9980001 | |
| Acute osteomyelitis of ulna (disorder) | 203166007 | |
| Multiple epiphyseal dysplasia Lowry type (disorder) | 768935003 | [A rare primary bone dysplasia with characteristics of small, flat epiphyses (especially the capital femoral epiphyses), rhizomelic shortening of limbs, cleft of secondary palate, micrognathia, mild joint contractures and facial dysmorphism (including mildly upward-slanting palpebral fissures, hypertelorism, broad nasal tip). Additionally reported features include scoliosis, genu valgum, mild pectus excavatum, platyspondyly, dislocated radial heads, brachydactyly, hypoplastic fibulae and talipes equinovarus.] |