Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Antigen of Human gammaherpesvirus 4 capsid protein (substance) | 103106005 | |
| Sexual inadequacy (finding) | 16124009 | |
| Reverse isolation nursing in positive pressure environment (regime/therapy) | 444909009 | |
| Chronic ectopic atrial tachycardia (disorder) | 26950008 | |
| 11-O-demethyl-17-O-deacetylvindoline O-methyltransferase (substance) | 130262000 | |
| Streptomyces echinatus (organism) | 440290001 | |
| Endogenous endophthalmitis caused by Aspergillus (disorder) | 1231258007 | |
| Aspergillus endophthalmitis (disorder) | 413583003 | |
| Monospot test positive (finding) | 302785009 | |
| Mid-brown constitutive skin color (finding) | 403241000 | |
| Segmental hypohidrosis (disorder) | 230661001 | |
| Acquired valgus deformity of right ankle (disorder) | 323431000119108 | |
| Umbilical cord stump cauterization (procedure) | 238251003 | |
| Cauterization of navel (procedure) | 2794006 | |
| Inpatient stay 2 days (finding) | 183800000 | |
| Middle ear fluid (substance) | 733753009 | |
| Hyperparakeratosis (morphologic abnormality) | 125554003 | |
| Suspicious behavior (finding) | 22927000 | |
| Cataract with aberrant oral frenula and growth delay syndrome (disorder) | 715988005 | [This syndrome is characterized by cataracts and short stature associated with variable anomalies, including aberrant oral frenula, a characteristic facial appearance (posteriorly angulated ears, upslanting palpebral fissures, small nose, ptosis and epicanthal folds) cavernous hemangiomas and hernias. It has been described in a mother and her two children. It is transmitted as an autosomal dominant trait., This syndrome is characterized by cataracts and short stature associated with variable anomalies, including aberrant oral frenula, a characteristic facial appearance (posteriorly angulated ears, upslanting palpebral fissures, small nose, ptosis and epicanthal folds) cavernous haemangiomas and hernias. It has been described in a mother and her two children. It is transmitted as an autosomal dominant trait.] |
| Entire left cerebellar hemisphere (body structure) | 1010601004 |