Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Planar tomography x-ray system table, powered (physical object) | 463955009 | |
| Stabbing self (finding) | 284759005 | |
| 60 minute serum cortisol measurement (procedure) | 313986002 | |
| Plain X-ray sacrum normal (finding) | 168584006 | |
| Hemoglobin Chiapas (substance) | 86336000 | |
| Light pressure touch, function (observable entity) | 247314007 | |
| Cholinergic angioedema (disorder) | 402411005 | |
| Entire cerebellar vermis (body structure) | 279105006 | |
| Prazosin measurement (procedure) | 121663004 | |
| Screenwash (substance) | 311913009 | |
| Product containing precisely sodium bicarbonate 50 milligram/1 milliliter conventional release solution for injection (clinical drug) | 784945000 | |
| Product containing precisely morphine sulfate 15 milligram/1 milliliter conventional release solution for injection (clinical drug) | 782007000 | |
| Rubus idaeus specific immunoglobulin E antibody measurement (procedure) | 397667000 | |
| Immunoglobulin gene GM allotype (substance) | 79005005 | |
| Hypothyroidism due to mutation in transcription factor of pituitary development (disorder) | 718194004 | [A permanent thyroid deficiency that is present from birth, characterised by low levels of thyroid hormones caused by disorders in the development or function of the pituitary. The clinical manifestations can be subtle, probably as a result of trans-placental passage of some maternal thyroid hormone or due to the fact that many infants have some thyroid production of their own. Goitre is always absent. Slow linear growth and developmental delay are usually apparent by 4-6 months of age. Without treatment hypothyroidism results in severe intellectual deficit and short stature. The hypothyroidism is caused by mutations in genes regulating pituitary gland development including HESX1, LHX3, LHX4, POU1F1 and PROP1 (3p21.2-p21.1, 9q34.3, 1q25, 3p11 and 5q)., A permanent thyroid deficiency that is present from birth, characterized by low levels of thyroid hormones caused by disorders in the development or function of the pituitary. The clinical manifestations can be subtle, probably as a result of trans-placental passage of some maternal thyroid hormone or due to the fact that many infants have some thyroid production of their own. Goiter is always absent. Slow linear growth and developmental delay are usually apparent by 4-6 months of age. Without treatment hypothyroidism results in severe intellectual deficit and short stature. The hypothyroidism is caused by mutations in genes regulating pituitary gland development including HESX1, LHX3, LHX4, POU1F1 and PROP1 (3p21.2-p21.1, 9q34.3, 1q25, 3p11 and 5q).] |
| Entire palpebral fissure (body structure) | 280576003 | |
| Use of prosthesis (attribute) | 260685000 | |
| Myeloid leukemia associated with Down Syndrome (morphologic abnormality) | 450935006 | |
| Deoxyribonucleic acid of Mycoplasma penetrans (substance) | 708380000 | |
| Genetic crossing over (finding) | 35147005 |