All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Small scrotum (finding) | 276332008 | |
| Insulin (porcine) specific immunoglobulin E (substance) | 388433000 | |
| Cerebrospinal fluid: microorganisms seen (finding) | 167725008 | |
| History of panretinal photocoagulation (situation) | 69741000119103 | |
| Sporadic primary amyloidosis (disorder) | 190923000 | |
| Product containing carteolol in ocular dose form (medicinal product form) | 769018006 | |
| Trimetazidine hydrochloride (substance) | 703366005 | |
| Plasma alpha-fetoprotein multiple of median measurement (procedure) | 313867006 | |
| Congenital dyserythropoietic anemia, type I (disorder) | 59548005 | |
| Congenital anomaly of second branchial cleft (disorder) | 1231169000 | [A rare otorhinolaryngological malformation with the presence of a cyst, sinus or fistula occurring along the anterior border of the sternocleidomastoid muscle. Second branchial cleft fistula and sinuses present with skin opening with chronic discharge and recurrent infections, whereas second branchial cleft cysts present as a painless, nontender, stable in size or slowly enlarging lateral neck masses. Cysts occasionally acutely increase in size during upper respiratory tract infection, leading to respiratory compromise, torticollis and dysphagia.] |
| Gluten-free bread mix (product) | 328682001 | |
| Life satisfaction index A (assessment scale) | 273572007 | |
| Bovine enterovirus 3 (organism) | 50074000 | |
| Cardiac akinesia (finding) | 195675009 | |
| Kelch like family member 9 related early-onset distal myopathy (disorder) | 763776004 | [A rare genetic distal myopathy with characteristics of slowly progressive distal limb muscle weakness and atrophy (beginning with anterior tibial muscle involvement followed by the intrinsic hand muscles) in association with reduced sensation in a stocking-glove distribution. Patients present with high stepping gait, ankle areflexia and contractures in the first to second decade of life, associated with marked ankle extensor muscle atrophy; later proximal muscle involvement is moderate and ambulation is preserved throughout the life.] |
| Congenital cardiac diverticulum (disorder) | 718181001 | [A very rare congenital malformation characterised by a muscular appendix emerging from the left ventricular apex, rarely from the right ventricle or from both chambers, with clinical manifestations ranging from asymptomatic to life-threatening haemodynamic collapse. Often associated with other cardiac abnormalities but is mostly an isolated anomaly. It is mostly found in infants and children and occasionally as an incidental finding in adults. Two types are described: fibrous and muscular. The aetiology of congenital cardiac diverticulum is not known. Haemodynamic factors may play a role., A very rare congenital malformation characterized by a muscular appendix emerging from the left ventricular apex, rarely from the right ventricle or from both chambers, with clinical manifestations ranging from asymptomatic to life-threatening hemodynamic collapse. Often associated with other cardiac abnormalities but is mostly an isolated anomaly. It is mostly found in infants and children and occasionally as an incidental finding in adults. Two types are described: fibrous and muscular. The etiology of congenital cardiac diverticulum is not known. Hemodynamic factors may play a role.] |
| Prorocentrum (organism) | 43717003 | |
| Spontaneous closure of residual interatrial communication (finding) | 459186008 | |
| Transection of muscle of pelvis (procedure) | 55747005 | |
| Amelogenesis imperfecta - hypomaturation - snow capped teeth (disorder) | 234966003 |