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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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Preferred Name | Hereditary Central Nervous System Demyelinating Diseases [Disease/Finding] | |
Synonyms |
Hereditary Central Nervous System Demyelinating Diseases Demyelinating Diseases, Central Nervous System, Hereditary Central Nervous System Hereditary Demyelinating Diseases Central Nervous System Demyelinating Diseases, Hereditary Demyelinating Central Nervous System Diseases, Hereditary Central Nervous System Demyelinating Hereditary Diseases Hereditary Demyelinating Diseases, Central Nervous System |
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ID |
http://purl.bioontology.org/ontology/NDFRT/N0000004096 |
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altLabel |
Hereditary Central Nervous System Demyelinating Diseases Demyelinating Diseases, Central Nervous System, Hereditary Central Nervous System Hereditary Demyelinating Diseases Central Nervous System Demyelinating Diseases, Hereditary Demyelinating Central Nervous System Diseases, Hereditary Central Nervous System Demyelinating Hereditary Diseases Hereditary Demyelinating Diseases, Central Nervous System
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cui |
C0751877
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MESH DEFINITION |
Inherited conditions characterized by a loss of MYELIN in the central nervous system.
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MESH DUI |
D020279
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MeSH name |
Hereditary Central Nervous System Demyelinating Diseases
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MESH UI |
M0328329
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NDFRT kind |
DISEASE_KIND
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notation |
N0000004096
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NUI |
N0000004096
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prefLabel |
Hereditary Central Nervous System Demyelinating Diseases [Disease/Finding]
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tui |
T047
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subClassOf |
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Mapping To | Ontology | Source |
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http://purl.bioontology.org/ontology/MSHFRE/D020279 | MSHFRE | CUI |
http://purl.bioontology.org/ontology/MESH/D020279 | MESH | CUI |