DOID:896: Difference between revisions
From FANTOM5_SSTAR
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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 | |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= | ||
|derives_from= | |derives_from= | ||
|develops_from= | |develops_from= |
Latest revision as of 16:33, 26 June 2012
Name: | metal metabolism disorder | ||
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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: |
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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) |
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Children
is a: | DOID:893 (Wilson disease) |
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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