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DOID:893

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Name:Wilson disease
Namespace:disease_ontology
Xrefs:
links:

MSH:D006527
NCI:C84756
OMIM:277900
SNOMEDCT_2010_1_31:154751003
SNOMEDCT_2010_1_31:190823004
SNOMEDCT_2010_1_31:191710006
SNOMEDCT_2010_1_31:192640001
SNOMEDCT_2010_1_31:267504005
SNOMEDCT_2010_1_31:88518009

UMLS_CUI:C0019202
Synonyms: "Cerebral pseudosclerosis (disorder)" EXACT [SNOMEDCT_2005_07_31:192640001]
"hepatolenticular degeneration" EXACT []
"Westphal pseudosclerosis" EXACT [CSP2005:1849-4349]
"Westphal-Strumpell syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:190823004]
"Wilson's disease" EXACT [SNOMEDCT_2005_07_31:267504005]
"Wilson's disease" EXACT [SNOMEDCT_2005_07_31:154751003]
"Wilson's disease" EXACT [MTHICD9_2006:275.1]
"Wilson's disease (disorder)" EXACT [SNOMEDCT_2005_07_31:88518009]
"Wilson's disease * (disorder)" EXACT [SNOMEDCT_2005_07_31:191710006]
Comments:OMIM mapping confirmed by DO. [SN].

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:409(liver disease),DOID:896(metal metabolism disorder)



Children


is a:FF:10578-108C2 (),FF:10579-108C3 (),FF:10582-108C6 ()

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:893 (Wilson disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data


No analysis results