DOID:11983: Difference between revisions
From FANTOM5_SSTAR
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|id=DOID:11983
|name=Prader-Willi syndrome
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|def=
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|is_a=DOID:0080014
|synonym="Prader - Willi syndrome" EXACT [SNOMEDCT_2005_07_31:205794007];;...") |
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|id=DOID:11983 | |id=DOID:11983 | ||
|name=Prader-Willi syndrome | |name=Prader-Willi syndrome | ||
|namespace= | |namespace=disease_ontology | ||
|def= | |def= | ||
|xref= | |xref=ICD9CM:759.81;;MSH:D011218;;NCI:C75463;;OMIM:176270;;SNOMEDCT_2010_1_31:205794007;;SNOMEDCT_2010_1_31:89392001;;UMLS_CUI:C0032897 | ||
|is_a=DOID:0080014 | |is_a=DOID:0080014 | ||
|synonym="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] | |synonym="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] | ||
|comment= | |comment=OMIM mapping confirmed by DO. [SN]. | ||
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|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo | |||
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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) |
|---|
Children
| is a: | FF:10521-107E8 () |
|---|
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
