Personal tools

DOID:0060158: Difference between revisions

From FANTOM5_SSTAR

Jump to: navigation, search
(Created page with "{{DOID |id=DOID:0060158 |name=acquired metabolic disease |namespace= |def="A disease of metabolism that has _material_basis_in enzyme deficiency or accumulation of enzymes...")
 
No edit summary
 
(One intermediate revision by the same user not shown)
Line 2: Line 2:
|id=DOID:0060158
|id=DOID:0060158
|name=acquired metabolic disease
|name=acquired metabolic disease
|namespace=
|namespace=disease_ontology
|def="A disease of metabolism that has _material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or malabsorption." [url:http\://en.wikipedia.org/wiki/Inborn_error_of_metabolism, url:http\://www.ncbi.nlm.nih.gov/mesh/68008659]
|def="A disease of metabolism that has _material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or malabsorption." [url:http://en.wikipedia.org/wiki/Inborn_error_of_metabolism, url:http://www.ncbi.nlm.nih.gov/mesh/68008659]
|xref=
|xref=
|is_a=DOID:0014667
|is_a=DOID:0014667
Line 14: Line 14:
|obo_creation_date=2011-08-24T02:53:03Z
|obo_creation_date=2011-08-24T02:53:03Z
|subset=
|subset=
|adjacent_to=
|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 16:31, 26 June 2012

Name:acquired metabolic disease
Namespace:disease_ontology
Definition:"A disease of metabolism that has _material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or malabsorption." [url:http://en.wikipedia.org/wiki/Inborn_error_of_metabolism, url:http://www.ncbi.nlm.nih.gov/mesh/68008659]
Created by:lschriml
Creation date:2011-08-24T02:53:03Z

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:0014667(disease of metabolism)



Children


is a:DOID:3650 (lactic acidosis)

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:0060158 (acquired metabolic disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data


No analysis results