DOID:896: Difference between revisions
From FANTOM5_SSTAR
(Created page with "{{DOID
|id=DOID:896
|name=inborn errors of metal metabolism
|namespace=
|def=
|xref=
|is_a=DOID:655
|synonym="inborn metal metabolism disorder" EXACT [CSP2005:4000-0215...") |
No edit summary |
||
| (One intermediate revision by the same user not shown) | |||
| Line 1: | Line 1: | ||
{{DOID | {{DOID | ||
|id=DOID:896 | |id=DOID:896 | ||
|name= | |name=metal metabolism disorder | ||
|namespace= | |namespace=disease_ontology | ||
|def= | |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= | |xref=MSH:D008664;;UMLS_CUI:C0025534 | ||
|is_a=DOID:655 | |is_a=DOID:655 | ||
|synonym="inborn metal metabolism disorder" EXACT [CSP2005:4000-0215] | |synonym="inborn metal metabolism disorder" EXACT [CSP2005:4000-0215] | ||
| Line 14: | Line 14: | ||
|obo_creation_date= | |obo_creation_date= | ||
|subset= | |subset= | ||
|derives_from= | |derives_from= | ||
|develops_from= | |develops_from= | ||
| Line 20: | Line 19: | ||
|located_in= | |located_in= | ||
|part_of= | |part_of= | ||
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo | |||
|is_obsolete= | |||
|preceded_by= | |||
}} | }} | ||
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: |
| ||
| 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
