Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Bagaza virus (organism) | 68096005 | |
| Structure of left round ligament of uterus (body structure) | 890308009 | |
| Brugia tupaiae (organism) | 7176004 | |
| Dysphasia due to and following embolic cerebrovascular accident (disorder) | 690351000119103 | |
| Dysphasia due to and following cerebrovascular accident (disorder) | 16260551000119106 | |
| Removal of foreign body from antecubital fossa (procedure) | 60836005 | |
| Cyanotic congenital heart disease (disorder) | 12770006 | |
| Entire inner preputial lamina (body structure) | 367698006 | |
| tablespoons/day (qualifier value) | 228951003 | |
| Onset of symptom speed (finding) | 162461008 | |
| Hiletron neutron external beam radiation therapy (procedure) | 228676000 | |
| Maternal effort during second stage of labor (finding) | 249161008 | |
| Periurethral route (qualifier value) | 418204005 | [A route that begins within or around the tissues surrounding the urethra.] |
| Eosinophil count normal (finding) | 165522008 | |
| Urophycis regia (organism) | 83984008 | |
| Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (disorder) | 720749004 | [A degenerative corneal disorder characterised by the association of congenital hereditary endothelial dystrophy with progressive postlingual sensorineural hearing loss. The ocular manifestations include diffuse bilateral corneal oedema occurring with severe corneal clouding, blurred vision, visual loss and nystagmus. Caused by mutations in the SLC4A11 gene located at the CHED2 locus on chromosome 20p13p12., A degenerative corneal disorder characterized by the association of congenital hereditary endothelial dystrophy with progressive postlingual sensorineural hearing loss. The ocular manifestations include diffuse bilateral corneal edema occurring with severe corneal clouding, blurred vision, visual loss and nystagmus. Caused by mutations in the SLC4A11 gene located at the CHED2 locus on chromosome 20p13p12.] |
| 5000000 (qualifier value) | 732779008 | |
| Abnormal pituitary follicle stimulating hormone (finding) | 131018009 | |
| Topical budesonide adverse reaction (disorder) | 293176006 | |
| Budesonide adverse reaction (disorder) | 293175005 |