DOID:225
From FANTOM5_SSTAR
Name: | syndrome | ||
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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: |
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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) |
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Children
is a: | FF:10772-110F7 (myelodysplastic syndrome cell line:SKM-1) |
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Ontology Tree: Loaded from BioPortal
Ontorolgy tree(Small window open)
FF samples
Human (Homo sapiens)
- 10772-110F7 (myelodysplastic syndrome cell line:SKM-1)
Mouse (Mus musculus)
- 10772-110F7 (myelodysplastic syndrome cell line:SKM-1)
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