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DOID:5688

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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)

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