Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Entire costocoracoid ligament (body structure) | 725144003 | |
| Product containing only papain (medicinal product) | 777061004 | |
| Chemically-induced proctitis (disorder) | 235759004 | |
| Chronic cicatrizing conjunctivitis due to Stevens-Johnson syndrome (disorder) | 1217675008 | |
| Total jejunectomy and anastomosis of duodenum to colon (procedure) | 173897003 | |
| Product containing midazolam in oromucosal dose form (medicinal product form) | 870494008 | |
| Foreign body giant cell (cell) | 21386001 | |
| Planococcus antarcticus (organism) | 432892008 | |
| Parenteral nutrition formula intake composition (observable entity) | 1209079002 | [The parenteral nutrition formula macronutrient distribution.] |
| Entire infratentorial region of cranial cavity (body structure) | 368556004 | |
| Serotype 4ab (qualifier value) | 264683004 | |
| Foscarnet adverse reaction (disorder) | 292842006 | |
| Child for adoption (finding) | 183434005 | |
| Decortication - action (qualifier value) | 129384000 | |
| Adjustment reaction of adolescence (disorder) | 386822001 | |
| Entire median lobe of prostate (body structure) | 245466000 | |
| Old subtotal retinal detachment (disorder) | 193327005 | |
| Primary peristaltic contraction of esophagus, function (observable entity) | 23431008 | |
| Revision fixation of fracture of vertebra with plate (procedure) | 301048006 | |
| Hereditary hyperekplexia (disorder) | 724351008 | [A hereditary neurological disorder with characteristics of excessive startle responses. The disease manifests shortly after birth with violent jerking to noise and touch, and massive and sustained stiffening of the trunk and limbs, clenching fists, and attacks of a high frequency trembling. Motor milestones are often mildly delayed, but intellectual development is usually normal. Mutations in the GLRA1 gene (5q32) are found in about 30% of patients. These mutations are transmitted as an autosomal dominant or recessive trait. The GLRA1 gene encodes the alpha1 subunit of the juvenile neuronal receptor for the inhibitory neurotransmitter, glycine. Mutations of this subunit cause a variety of dysfunctions of the neuronal chloride (Cl-) channel. Mutations in the GLRB, GPHN and SLC6A5 genes (4q31.3, 14q24 and 11p15.2-p15.1) have also been observed.] |