Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Health of the Nation Outcome Scale item 5 - physical illness/disability (assessment scale) | 281119001 | |
| Neoplaconema (organism) | 419613008 | |
| Melanoma in situ of skin of right lower eyelid (disorder) | 16907241000119105 | |
| Chameleon (organism) | 40931007 | |
| Resorption of lumbar disc (disorder) | 202754001 | |
| Closure by wire (procedure) | 14133008 | |
| Developmental academic disorder due to nutritional stunting (disorder) | 1186823002 | |
| Impairment of peripheral tissue perfusion (finding) | 704449003 | |
| Oklahoma (geographic location) | 420626004 | |
| Infarction of spinal cord (disorder) | 432249006 | |
| Garlic breath (finding) | 30276000 | |
| Lumbosacral spine orthosis, pendulous abdomen support (physical object) | 470010001 | |
| Phalaris arundinacea diagnostic allergen extract (product) | 411789005 | |
| Neoplasm of uncertain behavior of trigone of urinary bladder (disorder) | 95149005 | |
| Product containing precisely tiotropium (as tiotropium bromide) 2.5 microgram/1 actuation conventional release solution for inhalation (clinical drug) | 1197458002 | |
| Rapid human immunodeficiency virus type 1 antibody test (procedure) | 409788009 | |
| Hyperplasia of islet alpha cells with glucagon excess (disorder) | 87181002 | |
| Toilet on hospital premises (environment) | 224889001 | |
| Antimitochondrial antibody titer (procedure) | 413070005 | |
| X-linked intellectual disability Hedera type (disorder) | 726727003 | [A rare X-linked intellectual disability syndrome characterized by onset in infancy of delayed motor and speech milestones, generalized tonic-clonic seizures and drop attacks and mild to moderate intellectual disability. Additional less common manifestations include scoliosis, ataxia (resulting in progressive gait disturbance) and bilateral pes planovalgus. Physical appearance is normal with no dysmorphic features reported., A rare X-linked intellectual disability syndrome characterised by onset in infancy of delayed motor and speech milestones, generalised tonic-clonic seizures and drop attacks and mild to moderate intellectual disability. Additional less common manifestations include scoliosis, ataxia (resulting in progressive gait disturbance) and bilateral pes planovalgus. Physical appearance is normal with no dysmorphic features reported.] |