DOID:893: Difference between revisions
From FANTOM5_SSTAR
(Created page with "{{DOID
|id=DOID:893
|name=Wilson disease
|namespace=
|def=
|xref=
|is_a=DOID:409;;DOID:896
|synonym="Cerebral pseudosclerosis (disorder)" EXACT [SNOMEDCT_2005_07_31:192...") |
No edit summary |
||
| Line 2: | Line 2: | ||
|id=DOID:893 | |id=DOID:893 | ||
|name=Wilson disease | |name=Wilson disease | ||
|namespace= | |namespace=disease_ontology | ||
|def= | |def= | ||
|xref= | |xref=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 | ||
|is_a=DOID:409;;DOID:896 | |is_a=DOID:409;;DOID:896 | ||
|synonym="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 [ | |synonym="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] | ||
|comment= | |comment=OMIM mapping confirmed by DO. [SN]. | ||
|alt_id= | |alt_id= | ||
|disjoint_from= | |disjoint_from= | ||
| Line 20: | Line 20: | ||
|located_in= | |located_in= | ||
|part_of= | |part_of= | ||
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo | |||
|is_obsolete= | |||
|preceded_by= | |||
}} | }} | ||
Revision as of 14:01, 11 June 2012
| Name: | Wilson disease | ||
|---|---|---|---|
| Namespace: | disease_ontology | ||
| Xrefs: |
| ||
| 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
