Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Endarterectomy and angioplasty of renal artery with prosthesis (procedure) | 405405000 | |
| Metformin hydrochloride (substance) | 109083009 | |
| Fusion protein BCR-ABL (substance) | 56564003 | |
| Injection of hormone for local action (procedure) | 1216948008 | |
| Referral to liaison nurse (procedure) | 306337008 | |
| Promegakaryocyte (cell) | 50284009 | |
| Streptococcus pyogenes type emm14 (organism) | 428541006 | |
| Epileptic aura (finding) | 57935008 | |
| Aura (finding) | 18618006 | |
| Laparoscopic gastroenterostomy (procedure) | 307195003 | |
| Hydraulic and/or pneumatic external ankle and/or foot prosthesis (physical object) | 870664005 | |
| Entire short sole muscle (body structure) | 727649008 | |
| Status of distant metastasis for primary extraosseous tumor (observable entity) | 409746000 | |
| Hepatic fibrosis, renal cyst, intellectual disability syndrome (disorder) | 771149000 | [A rare syndromic intellectual disability characterized by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnea. There have been no further descriptions in the literature since 1987., A rare syndromic intellectual disability characterised by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnoea. There have been no further descriptions in the literature since 1987.] |
| Articulation disorder due to hyperkinesis (disorder) | 427145007 | |
| Presence of primary malignant neoplasm of pharynx at surgical margin in excised tissue specimen (observable entity) | 1156487003 | |
| Narcissistic personality disorder (disorder) | 80711002 | |
| Dasabuvir sodium (substance) | 716018007 | |
| Entire canine region of oral cavity (body structure) | 730797009 | |
| Primary pigmented nodular adrenocortical disease (disorder) | 719274008 | [Primary pigmented nodular adrenocortical disease (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal sized adrenal glands containing multiple small cortical pigmented nodules. A substantial proportion of patients present during early childhood (2-3 years). More than 90% of reported cases of PPNAD occur as one of the manifestations of Carney complex. The condition is inherited in an autosomal dominant manner and can be associated with mutations in the PRKAR1A, PDE11A and PDE8B genes.] |