DOID:5688
From FANTOM5_SSTAR
| Name: | Werner syndrome | ||
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| Namespace: | disease_ontology | ||
| Xrefs: |
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| Synonyms: |
"adult premature ageing syndrome" EXACT [SNOMEDCT_2005_07_31:190590004] "adult progeria" EXACT [CSP2005:1849-9804] "Werner syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:51626007] "Werner's syndrome" EXACT [MTHICD9_2006:259.8] "Werner's syndrome" EXACT [SNOMEDCT_2005_07_31:190592007] "WS" EXACT [NCI2004_11_17:C3447] | ||
| Comments: | OMIM mapping confirmed by DO. [LS]. |
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:0050177(monogenic disease) |
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Children
| is a: | FF:10584-108C8 () |
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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:5688 (Werner syndrome), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data
No analysis results
