Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Islet cell adenomatosis (disorder) | 274944000 | |
| Withdrawing motor response to command (finding) | 298333003 | |
| Accidental ingestion of bog bilberries (event) | 242313008 | |
| Discharge from orthopedic service (procedure) | 306668002 | |
| Zinc polycarboxylate dental cement (substance) | 277873005 | |
| Confusion, urea, respiratory rate, blood pressure, 65 years of age or older score (assessment scale) | 445019007 | |
| Nasal chondrotomy (procedure) | 42213007 | |
| Scriver-Goldbloom-Roy syndrome (disorder) | 5078000 | |
| Acquired absence of lens of eye (disorder) | 1208877008 | |
| Removal of bladder calculus by urethral catheter suction (procedure) | 176194004 | |
| Tarsal wedge resection of upper eyelid (procedure) | 231614006 | |
| Feathery degeneration (morphologic abnormality) | 19438006 | |
| Entire superior wall of orbit (body structure) | 362643007 | |
| Conversion of static cast brace to functional cast brace (procedure) | 239704005 | |
| Vasospasm reflex (observable entity) | 386719008 | |
| Arachis hypogaea (organism) | 75413007 | |
| Protamine adverse reaction (disorder) | 292739008 | |
| Adverse reaction caused by anticoagulant antagonists (disorder) | 218572006 | |
| Closed traumatic subluxation radiocarpal joint (disorder) | 208839008 | |
| Hemochromatosis type 3 (disorder) | 719974003 | [A form of rare hereditary haemochromatosis, a group of diseases characterised by excessive tissue iron deposition of genetic origin. Type 3 haemochromatosis concerns middle aged-adults but also adolescents and young adults. It presents with liver disease, hypogonadism, arthritis, diabetes and skin pigmentation. The disease is caused by mutations of the transferrin receptor 2 gene (TFR2) on chromosome 7. Transmission is autosomal recessive., A form of rare hereditary hemochromatosis, a group of diseases characterized by excessive tissue iron deposition of genetic origin. Type 3 hemochromatosis concerns middle aged-adults but also adolescents and young adults. It presents with liver disease, hypogonadism, arthritis, diabetes and skin pigmentation. The disease is caused by mutations of the transferrin receptor 2 gene (TFR2) on chromosome 7. Transmission is autosomal recessive.] |