Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Persistent embryonic otic artery (disorder) | 253196005 | |
| Persistent cerebral embryonic artery (disorder) | 234123009 | |
| Entire right epididymis (body structure) | 367723004 | |
| Product containing idebenone in oral dose form (medicinal product form) | 1157292008 | |
| Metageria (disorder) | 238871000 | |
| Phage type Scarborough (qualifier value) | 303225002 | |
| Bluetongue virus 12 (organism) | 50838008 | |
| Wallis and Futuna islands (geographic location) | 223410008 | |
| Structure of permanent upper lateral incisor tooth socket (body structure) | 280484001 | |
| BL10 (body structure) | 272887002 | |
| Ear, nose and throat stereotactic surgery system (physical object) | 468890004 | |
| Mother smokes (situation) | 161078008 | |
| X-linked intellectual disability Shrimpton type (disorder) | 718905007 | [This syndrome is characterized by the association of severe intellectual deficit with microcephaly, strabismus and short stature. It has been described in three boys from two unrelated families. Transmission is X-linked recessive and the causative gene has been localized to the q12-Xq21.31 region of the X-chromosome., This syndrome is characterised by the association of severe intellectual deficit with microcephaly, strabismus and short stature. It has been described in three boys from two unrelated families. Transmission is X-linked recessive and the causative gene has been localised to the q12-Xq21.31 region of the X-chromosome.] |
| Blood group antibody D 1276 (substance) | 5064001 | |
| Palinopsia (finding) | 25462005 | |
| Multiple visual images (finding) | 246654007 | |
| Verbal consent for examination (finding) | 415812007 | |
| Debridement of open fracture of femur (procedure) | 81203002 | |
| Gallate 1-beta-glucosyltransferase (substance) | 73606003 | |
| Conventional release solution for oral drops (dose form) | 385019009 |