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DOID:331

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Name:central nervous system disease
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:
links:

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

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)



Children


is a:DOID:1289 (neurodegenerative disease),DOID:936 (brain disease)

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