DOID:331: Difference between revisions
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|name=central nervous system disease | |name=central nervous system disease | ||
|namespace=disease_ontology | |namespace=disease_ontology | ||
|def="A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system." [url:http | |def="A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system." [url:http://en.wikipedia.org/wiki/Central_nervous_system_disease] | ||
|xref=MSH:D002493;;NCI:C2934;;SNOMEDCT_2010_1_31:138748005;;SNOMEDCT_2010_1_31:154981003;;SNOMEDCT_2010_1_31:155049004;;SNOMEDCT_2010_1_31:155059003;;SNOMEDCT_2010_1_31:192641002;;SNOMEDCT_2010_1_31:193076009;;SNOMEDCT_2010_1_31:194566008;;SNOMEDCT_2010_1_31:23853001;;SNOMEDCT_2010_1_31:267144009;;SNOMEDCT_2010_1_31:267679005;;SNOMEDCT_2010_1_31:267700003;;SNOMEDCT_2010_1_31:267702006;;SNOMEDCT_2010_1_31:275539005;;UMLS_CUI:C0007682 | |xref=MSH:D002493;;NCI:C2934;;SNOMEDCT_2010_1_31:138748005;;SNOMEDCT_2010_1_31:154981003;;SNOMEDCT_2010_1_31:155049004;;SNOMEDCT_2010_1_31:155059003;;SNOMEDCT_2010_1_31:192641002;;SNOMEDCT_2010_1_31:193076009;;SNOMEDCT_2010_1_31:194566008;;SNOMEDCT_2010_1_31:23853001;;SNOMEDCT_2010_1_31:267144009;;SNOMEDCT_2010_1_31:267679005;;SNOMEDCT_2010_1_31:267700003;;SNOMEDCT_2010_1_31:267702006;;SNOMEDCT_2010_1_31:275539005;;UMLS_CUI:C0007682 | ||
|is_a=DOID:863 | |is_a=DOID:863 | ||
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|obo_creation_date= | |obo_creation_date= | ||
|subset= | |subset= | ||
|derives_from= | |derives_from= | ||
|develops_from= | |develops_from= | ||
Revision as of 16:32, 26 June 2012
| Name: | central nervous system disease | ||
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| Namespace: | disease_ontology | ||
| Definition: | "A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system." [url:http://en.wikipedia.org/wiki/Central_nervous_system_disease] | ||
| Xrefs: |
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Ontology association<br>Each term has an is_a parent in the Disease Ontology, which has a linkage to an another entity and FANTOM5 samples.Libraries were grouped into mutually exclusive facets according to the FANTOM5 sample ontology mapping to DISEASE ontologies.<br><br>link to ontology dataset<br>data
Parents
| is_a: | DOID:863(nervous system disease) |
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Children
| is a: | DOID:1289 (neurodegenerative disease),DOID:936 (brain disease) |
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Ontology Tree: Loaded from BioPortal
Ontorolgy tree(Small window open)
FF samples
Human (Homo sapiens)
Mouse (Mus musculus)
Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:331 (central nervous system disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data
No analysis results
