Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Able to remember old motor skills (finding) | 285222000 | |
| Finding related to ability to remember old motor skills (finding) | 365904001 | |
| Malignant neoplasm of lower lip, external (disorder) | 187604008 | |
| Free soft dentoalveolar tissue graft procedure, including donor site (procedure) | 16481005 | |
| Helium+oxygen cylinder (physical object) | 337547003 | |
| Powder for conventional release nebulizer solution (dose form) | 385201005 | |
| Textile waterproofer (occupation) | 41448004 | |
| Human immunodeficiency virus 2 protein 15 antibody (substance) | 444554000 | |
| Chlamydia trachomatis, serotype I (organism) | 115296004 | |
| History of evisceration of eye proper (situation) | 113621000119107 | |
| Dysarthria of velopharynx (finding) | 229691009 | |
| Fine needle aspiration biopsy of soft tissue using ultrasonographic guidance (procedure) | 719895009 | |
| Stercorarius pomarinus (organism) | 57345000 | |
| Speech exercises (regime/therapy) | 311664007 | |
| Intellectual disability with strabismus syndrome (disorder) | 773405004 | [A rare genetic syndromic intellectual disability disorder characterised by moderate to severe intellectual disability and esotropia. Other associated features may include growth failure (underweight, failure to thrive, short stature), microcephaly, tone abnormalities (hypotonia, spasticity), epilepsy, behavioural problems (hyperactivity, aggressiveness), and/or abnormal brain morphology, including arachnoid cyst, cerebral atrophy, mild ventriculomegaly, and abnormal central nervous system myelination or corpus callosum agenesis. There is evidence the disease is caused by homozygous mutation in the ADAT3 gene on chromosome 19p13., A rare genetic syndromic intellectual disability disorder characterized by moderate to severe intellectual disability and esotropia. Other associated features may include growth failure (underweight, failure to thrive, short stature), microcephaly, tone abnormalities (hypotonia, spasticity), epilepsy, behavioral problems (hyperactivity, aggressiveness), and/or abnormal brain morphology, including arachnoid cyst, cerebral atrophy, mild ventriculomegaly, and abnormal central nervous system myelination or corpus callosum agenesis. There is evidence the disease is caused by homozygous mutation in the ADAT3 gene on chromosome 19p13.] |
| Deoxyribonucleic acid analysis, antenatal, blood (procedure) | 2898000 | |
| Cephalometric gonion to gnathion plane (body structure) | 5851000124105 | [The bony contour of the angle of the mandible, a line not a point.] |
| Thrombosis of transplanted vein (disorder) | 234045008 | |
| Transuterine pelvic venogram (procedure) | 241259009 | |
| Sprain of ligament of left sternoclavicular joint (disorder) | 11817301000119105 |