Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Advanced retinal disease due to diabetes mellitus (disorder) | 311782002 | |
| Intentional ethambutol overdose (disorder) | 296801006 | |
| Intentional ethambutol poisoning (disorder) | 291683008 | |
| Anatomic narrow angle glaucoma of bilateral eyes (disorder) | 346861000119107 | |
| Adult 55 year screening (procedure) | 171310001 | |
| Hemoglobin J-Camaguey (substance) | 9695001 | |
| Frail elderly (finding) | 404904002 | |
| Frailty (finding) | 248279007 | |
| Diaemus youngi (organism) | 392111003 | |
| Main spoken language Patois (finding) | 408534005 | |
| Losartan (substance) | 373567002 | |
| Infection caused by Leptospira Grippotyphosa (disorder) | 70543009 | |
| Family history of chronic ulcerative proctitis (situation) | 430729009 | |
| Corneal graft vascularization (disorder) | 314554007 | |
| Caregiver willing to share care with professionals (finding) | 224493002 | |
| Catheter slitter (physical object) | 467547008 | |
| Meningococcal retrobulbar neuritis (disorder) | 1089801000119108 | |
| Charcot-Marie-Tooth disease type 4B1 (disorder) | 715803003 | [Charcot-Marie-Tooth disease, type 4B1 (CMT4B1) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. It was initially described in an Italian family and around 10 additional families have been described so far. Onset occurs during early childhood with distal and proximal muscular weakness starting in the lower extremities, sensory loss and cranial nerve involvement. Foot deformities are frequent and diaphragmatic and facial involvement has been reported. CMT4B1 is caused by mutations in the gene encoding myotubularin-related protein 2 (MTMR2; 11q22), involved in polyphosphoinositide signaling. Transmitted in an autosomal recessive manner.] |
| Hidromeiosis (finding) | 366008 | |
| Diminished sweating (finding) | 111980002 |