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DOID:896: Difference between revisions

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|name=metal metabolism disorder
|name=metal metabolism disorder
|namespace=disease_ontology
|namespace=disease_ontology
|def="An inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals." [url:http\://en.wikipedia.org/wiki/Inborn_errors_of_metal_metabolism]
|def="An inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals." [url:http://en.wikipedia.org/wiki/Inborn_errors_of_metal_metabolism]
|xref=MSH:D008664;;UMLS_CUI:C0025534
|xref=MSH:D008664;;UMLS_CUI:C0025534
|is_a=DOID:655
|is_a=DOID:655
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|obo_creation_date=
|obo_creation_date=
|subset=
|subset=
|adjacent_to=
|derives_from=
|derives_from=
|develops_from=
|develops_from=

Latest revision as of 16:33, 26 June 2012

Name:metal metabolism disorder
Namespace:disease_ontology
Definition:"An inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals." [url:http://en.wikipedia.org/wiki/Inborn_errors_of_metal_metabolism]
Xrefs:
links:

MSH:D008664

UMLS_CUI:C0025534
Synonyms: "inborn metal metabolism disorder" EXACT [CSP2005:4000-0215]

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:893 (Wilson disease)

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:896 (metal 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