DOID:11983: Difference between revisions
From FANTOM5_SSTAR
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Latest revision as of 16:31, 26 June 2012
| Name: | Prader-Willi syndrome | ||
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| Namespace: | disease_ontology | ||
| Xrefs: |
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| Synonyms: |
"Prader - Willi syndrome" EXACT [SNOMEDCT_2005_07_31:205794007] "Prader Willi syndrome" EXACT [CSP2005:1849-7731] "Prader-Willi syndrome" EXACT [ICD9CM_2006:759.81] "Prader-Willi syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:89392001] | ||
| 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:0080014(chromosomal disease) |
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Children
| is a: | FF:10521-107E8 () |
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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:11983 (Prader-Willi syndrome), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data
No analysis results
