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DOID:3146: Difference between revisions

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(Created page with "{{DOID |id=DOID:3146 |name=inborn errors lipid metabolism |namespace= |def= |xref= |is_a=DOID:655 |synonym= |comment= |alt_id= |disjoint_from= |union_of= |created_...")
 
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{{DOID
{{DOID
|id=DOID:3146
|id=DOID:3146
|name=inborn errors lipid metabolism
|name=lipid metabolism disorder
|namespace=
|namespace=disease_ontology
|def=
|def="An inhertited metabolic disorder that involves the creation and degradation of lipids." [url:http\://en.wikipedia.org/wiki/Lipid_metabolism]
|xref=
|xref=MSH:D008052;;UMLS_CUI:C0023772
|is_a=DOID:655
|is_a=DOID:655
|synonym=
|synonym="fatty acid metabolism" EXACT []
|comment=
|comment=
|alt_id=
|alt_id=
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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 14:00, 11 June 2012

Name:lipid metabolism disorder
Namespace:disease_ontology
Definition:"An inhertited metabolic disorder that involves the creation and degradation of lipids." [url:http\://en.wikipedia.org/wiki/Lipid_metabolism]
Xrefs:
links:

MSH:D008052

UMLS_CUI:C0023772
Synonyms: "fatty acid metabolism" EXACT []

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:655(inherited metabolic disorder)



Children


is a:DOID:10583 (lipoidosis)

Ontology Tree: Loaded from BioPortal

Ontorolgy tree(Small window open)

FF samples

Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:3146 (lipid metabolism disorder), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data


No analysis results