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DOID:225

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Name:syndrome
Namespace:disease_ontology
Definition:"A disease comprised of a group of signs and symptoms that occur together and characterize a particular abnormality." [URL:http\://www2.merriam-webster.com/cgi-bin/mwmednlm?book=Medical&va=syndrome]
Xrefs:
links:

MSH:D013577
NCI:C28193
SNOMEDCT_2010_1_31:64572001

UMLS_CUI:C0039082
Synonyms: "syndrome" EXACT [MTH:NOCODE]
"syndrome, NOS" EXACT [SNOMEDCT_2005_07_31:64572001]

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:4(disease)



Children


is a:FF:10772-110F7 (myelodysplastic syndrome cell line:SKM-1)

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:225 (syndrome), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data