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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
Acronym | NDFRT |
Visibility | Public |
Description | National Drug File - Reference Terminology Public Inferred Edition, 2008_03_11 |
Status | Production |
Format | UMLS |
Contact | Michael J. Lincoln MD, michael.lincoln@va.gov |
Categories | Health |
Groups | Unified Medical Language System |
License Information | This ontology is made available via the UMLS. Users of all UMLS ontologies must abide by the terms of the UMLS license. |
Version | Released | Uploaded |
---|---|---|
NDFRT_2018_02_05_18_03_05 (Parsed, Indexed, Metrics, Annotator, Error Diff) | 05/07/2018 | 07/06/2018 |
2017AB (Archived) | 11/06/2017 | 07/06/2018 |
2017AA (Archived) | 05/08/2017 | 04/06/2018 |
2016AB (Archived) | 02/06/2017 | 02/06/2017 |
2016AA (Archived) | 09/06/2016 | 09/06/2016 |
2015AB (Archived) | 07/20/2016 | 07/20/2016 |
2015AA (Archived) | 06/09/2015 | 06/09/2015 |
2014AB (Archived) | 01/29/2015 | 01/29/2015 |
2014AA (Archived) | 05/28/2014 | 05/28/2014 |
2013AB (Archived) | 02/18/2014 | 02/18/2014 |
2013AA (Archived) | 01/14/2014 | 01/14/2014 |
2013AA (Archived) | 05/08/2013 | 09/25/2013 |
2008_03_11 (Archived) | 03/11/2008 | 07/31/2009 |
more... |
- National Drug File – Reference Terminology
- Logically inferred version in OWL of the National Drug File – Reference Terminology (NDF-RT). NDF-RT is the terminology used by FDA and the FedMed collaboration to code these essential pharmacologic properties of medications: Mechanism of Action, Physiologic Effect, Structural Class.
Classes | 36,202 |
Individuals | 0 |
Properties | 53 |
Maximum depth | 11 |
Maximum number of children | 953 |
Average number of children | 3 |
Classes with a single child | 4,051 |
Classes with more than 25 children | 87 |
Classes with no definition | 36,171 |
Jump to:
Id | http://purl.bioontology.org/ontology/NDFRT/N0000003300
http://purl.bioontology.org/ontology/NDFRT/N0000003300
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Preferred Name | Lambert-Eaton Myasthenic Syndrome [Disease/Finding] |
Synonyms |
Eaton-Lambert Myasthenic Syndrome
Myopathic-Myasthenic Syndrome of Eaton-Lambert
Eaton-Lambert Syndrome
Myasthenic Syndrome, Lambert-Eaton
Myasthenic-Myopathic Syndrome of Lambert-Eaton
Myasthenic-Myopathic Syndrome of Eaton-Lambert
Lambert-Eaton Syndrome
Lambert-Eaton Myasthenic Syndrome
Myopathic-Myasthenic Syndrome of Lambert-Eaton
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
altLabel |
Eaton-Lambert Myasthenic Syndrome
Myopathic-Myasthenic Syndrome of Eaton-Lambert
Eaton-Lambert Syndrome
Myasthenic Syndrome, Lambert-Eaton
Myasthenic-Myopathic Syndrome of Lambert-Eaton
Myasthenic-Myopathic Syndrome of Eaton-Lambert
Lambert-Eaton Syndrome
Lambert-Eaton Myasthenic Syndrome
Myopathic-Myasthenic Syndrome of Lambert-Eaton
See more
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prefLabel | Lambert-Eaton Myasthenic Syndrome [Disease/Finding]
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notation | N0000003300
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May be treated by | |
MESH DEFINITION | An autoimmune disease characterized by weakness and fatigability of proximal muscles, particularly of the pelvic girdle, lower extremities, trunk, and shoulder girdle. There is relative sparing of extraocular and bulbar muscles. CARCINOMA, SMALL CELL of the lung is a frequently associated condition, although other malignancies and autoimmune diseases may be associated. Muscular weakness results from impaired impulse transmission at the NEUROMUSCULAR JUNCTION. Presynaptic calcium channel dysfunction leads to a reduced amount of acetylcholine being released in response to stimulation of the nerve. (From Adams et al., Principles of Neurology, 6th ed, pp 1471)
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MESH UI | M0023968
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subClassOf | |
Semantic type UMLS property | |
MeSH name | Lambert-Eaton Myasthenic Syndrome
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NDFRT kind | DISEASE_KIND
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type | |
SNOMED CID | 56989000
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tui | T047
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NUI | N0000003300
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cui | C0022972
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MESH DUI | D015624
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