DOID:5679: Difference between revisions
From FANTOM5_SSTAR
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|name=retinal disease
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|is_a=DOID:5614
|synonym="retina disorder" EXACT [CSP2005:1114-9311];;"Retinal disorder" EXACT [NCI2...") |
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|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo | |||
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|synonym="retina disorder" EXACT [CSP2005:1114-9311];;"Retinal disorder" EXACT [NCI2004_11_17:C26875];;"Retinopathy (disorder)" EXACT [SNOMEDCT_2005_07_31:399625000] | |||
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|xref=ICD9CM:362.9;;MSH:D012164;;NCI:C26875;;NCI:C62601;;SNOMEDCT_2010_1_31:193430004;;SNOMEDCT_2010_1_31:267715002;;SNOMEDCT_2010_1_31:29555009;;SNOMEDCT_2010_1_31:35426003;;SNOMEDCT_2010_1_31:399625000;;UMLS_CUI:C0035309 | |||
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Latest revision as of 16:52, 12 September 2014
| Name: | retinal disease | ||
|---|---|---|---|
| Namespace: | FANTOM | ||
| Xrefs: |
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| Synonyms: |
"retina disorder" EXACT [CSP2005:1114-9311] "Retinal disorder" EXACT [NCI2004_11_17:C26875] "Retinopathy (disorder)" EXACT [SNOMEDCT_2005_07_31:399625000] |
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:5614(eye disease) |
|---|
Children
| is a: | DOID:4645 (retinal cancer) |
|---|
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:5679 (retinal disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data
No analysis results
