DOID:5688

Name:	Werner syndrome
Namespace:	disease_ontology
Xrefs:	links: MSH:D014898 NCI:C3447 OMIM:277700 SNOMEDCT_2010_1_31:190590004 SNOMEDCT_2010_1_31:190592007 SNOMEDCT_2010_1_31:51626007 UMLS_CUI:C0043119
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)

Children

is a:	FF:10584-108C8 ()

Ontology Tree: Loaded from BioPortal

Ontorolgy tree(Small window open)

FF samples

Human (Homo sapiens)

• 10584-108C8

Mouse (Mus musculus)

• 10584-108C8

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