Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Didymella aurea (organism) | 785779004 | |
| Blood group antibody Os^a^ (substance) | 83078008 | |
| Decreased cerebrospinal fluid formation (finding) | 20710005 | |
| Uridine diphosphate-N-acetylmuramate-alanine ligase (substance) | 2370009 | |
| Mucinous cystadenoma of right ovary (disorder) | 10871451000119105 | |
| Reversible ischemia of testis due to torsion of testis (disorder) | 1148916009 | |
| 17q12 microdeletion syndrome (disorder) | 733519008 | [A rare chromosomal anomaly syndrome resulting from the partial deletion of the long arm of chromosome 17. The disease is characterised by renal cystic disease, maturity onset diabetes of the young type 5 and neurodevelopmental disorders, such as cognitive impairment, developmental delay (particularly of speech), autistic traits and autism spectrum disorder. Mullerian aplasia in females, macrocephaly, mild facial dysmorphism (high forehead, deep set eyes and chubby cheeks) and transient hypercalcaemia has also been reported., A rare chromosomal anomaly syndrome resulting from the partial deletion of the long arm of chromosome 17. The disease is characterized by renal cystic disease, maturity onset diabetes of the young type 5 and neurodevelopmental disorders, such as cognitive impairment, developmental delay (particularly of speech), autistic traits and autism spectrum disorder. Mullerian aplasia in females, macrocephaly, mild facial dysmorphism (high forehead, deep set eyes and chubby cheeks) and transient hypercalcemia has also been reported.] |
| Persistent cough after viral respiratory infection (disorder) | 445241004 | |
| Persistent cough (finding) | 284523002 | |
| Autosomal semi-dominant severe lipodystrophic laminopathy (disorder) | 1197747005 | [A rare familial partial lipodystrophy with characteristics of severe partial lipoatrophy affecting the limbs, trunk, and abdomen, together with faciocervical fat accumulation. Additional manifestations include diabetes, acanthosis nigricans, liver steatosis and hypertriglyceridemia, as well as low serum leptin and adiponectin levels. Severe cardiac rhythm and conduction disturbances have also been reported., A rare familial partial lipodystrophy with characteristics of severe partial lipoatrophy affecting the limbs, trunk, and abdomen, together with faciocervical fat accumulation. Additional manifestations include diabetes, acanthosis nigricans, liver steatosis and hypertriglyceridaemia, as well as low serum leptin and adiponectin levels. Severe cardiac rhythm and conduction disturbances have also been reported.] |
| Myokymia, hyperhidrosis, impaired muscle relaxation syndrome (disorder) | 250081005 | |
| Appearance of gingivae (observable entity) | 364124005 | |
| Gingivae feature (observable entity) | 364123004 | |
| Collision of aircraft with another aircraft, while in transit, occupant of unpowered aircraft, except parachutist, injured (event) | 216015000 | |
| Campylobacter hyointestinalis subspecies lawsonii (organism) | 432459009 | |
| Peroxy acid device sterilant, organic (physical object) | 700687008 | |
| Structure of pedicle of eighth thoracic vertebra (body structure) | 68899002 | |
| Somali language (qualifier value) | 297306000 | |
| Brassica sativus var. longipinnatus (organism) | 28300004 | |
| Revision of total replacement of hip joint using metal augmentation (procedure) | 1230047003 |