DOID:893: Difference between revisions
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Latest revision as of 16:33, 26 June 2012
| Name: | Wilson disease | ||
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| Namespace: | disease_ontology | ||
| Xrefs: |
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| 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) |
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Children
| is a: | FF:10578-108C2 (),FF:10579-108C3 (),FF:10582-108C6 () |
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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: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
