All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| GV19 (body structure) | 273086003 | |
| Allergy to phenoperidine (finding) | 293607002 | |
| Product containing only alanylglutamine (medicinal product) | 774447008 | |
| Blepharonasofacial malformation syndrome (disorder) | 717913006 | [A rare otorhinolaryngological malformation syndrome with characteristics of a distinctive mask-like facial dysmorphism, lacrimal duct obstruction, extrapyramidal features, digital malformations and intellectual disability. Reported in 3 families to date. The facies has a mask-like appearance due to weakness of facial muscles and lacrimal duct obstruction is characteristic. Clinical features also include telecanthus, bulky nose, broad nasal bridge, sometimes a hypoplastic midface, longitudinal cheek furrows, trapezoidal upper lip and malformation of the ears. Intellectual disability, cutaneous syndactyly, torsion dystonia, increased deep tendon reflexes; Babinski sign, poor coordination and joint laxity are also observed.] |
| Tick paralysis (disorder) | 74225001 | |
| Chloramine B (substance) | 95987001 | |
| Bambara language (qualifier value) | 297723006 | |
| Absence of guilt (situation) | 102905003 | |
| Cerebral cysticercosis (disorder) | 230215006 | |
| Sandwich intake (observable entity) | 230083003 | |
| Soft tissue crepitus (finding) | 271776004 | |
| Cheek biting (finding) | 59901004 | |
| Intravascular catheter adaptor (physical object) | 469617006 | |
| Product containing ambenonium in oral dose form (medicinal product form) | 767864009 | |
| Ligation of internal jugular vein (procedure) | 7017002 | |
| Product containing precisely cetylpyridinium chloride 1 milligram/1 gram and lidocaine hydrochloride 3.3 milligram/1 gram conventional release dental gel (clinical drug) | 331263003 | |
| Does get on to toilet (finding) | 301546002 | |
| Rhizomelic syndrome Urbach type (disorder) | 770948004 | [A rare primary bone dysplasia characterized by upper limbs rhizomelia and other skeletal anomalies (for example short stature, dislocated hips, digitalization of the thumb with bifid distal phalanx), craniofacial features (for example microcephaly, large anterior fontanelle, fine and sparse scalp hair, depressed nasal bridge, high arched palate, micrognathia, short neck), congenital heart defects (for example pulmonary stenosis), delayed psychomotor development and mild flexion contractures of elbows. Radiologic evaluation may reveal flared epiphyses, platyspondyly and/or digital anomalies., A rare primary bone dysplasia characterised by upper limbs rhizomelia and other skeletal anomalies (for example short stature, dislocated hips, digitalisation of the thumb with bifid distal phalanx), craniofacial features (for example microcephaly, large anterior fontanelle, fine and sparse scalp hair, depressed nasal bridge, high arched palate, micrognathia, short neck), congenital heart defects (for example pulmonary stenosis), delayed psychomotor development and mild flexion contractures of elbows. Radiologic evaluation may reveal flared epiphyses, platyspondyly and/or digital anomalies.] |
| Disability evaluation disability 20 percent (finding) | 11411001 | |
| Adjustment of arteriovenous fistula stent (procedure) | 233488000 |