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(Created page with "{{DOID |id=DOID:5688 |name=Werner syndrome |namespace= |def= |xref= |is_a=DOID:0050177 |synonym="adult premature ageing syndrome" EXACT [SNOMEDCT_2005_07_31:190590004];...")
 
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|id=DOID:5688
|id=DOID:5688
|name=Werner syndrome
|name=Werner syndrome
|namespace=
|namespace=disease_ontology
|def=
|def=
|xref=
|xref=MSH:D014898;;NCI:C3447;;OMIM:277700;;SNOMEDCT_2010_1_31:190590004;;SNOMEDCT_2010_1_31:190592007;;SNOMEDCT_2010_1_31:51626007;;UMLS_CUI:C0043119
|is_a=DOID:0050177
|is_a=DOID:0050177
|synonym="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]
|synonym="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]
|comment=
|comment=OMIM mapping confirmed by DO. [LS].
|alt_id=
|alt_id=
|disjoint_from=
|disjoint_from=
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|located_in=
|located_in=
|part_of=
|part_of=
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo
|is_obsolete=
|preceded_by=
}}
}}

Revision as of 14:01, 11 June 2012

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