DOID:74: Difference between revisions
From FANTOM5_SSTAR
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|id=DOID:74
|name=hematopoietic system disease
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|is_a=DOID:1287
|synonym="Blood disease" EXACT [SNOMEDCT_2005_07_31:154785002];;"blood di...") |
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|id=DOID:74 | |id=DOID:74 | ||
|name=hematopoietic system disease | |name=hematopoietic system disease | ||
|namespace= | |namespace=disease_ontology | ||
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|xref= | |xref=ICD9CM:280-289.99;;ICD9CM:289.9;;MSH:D006402;;SNOMEDCT_2010_1_31:154785002;;SNOMEDCT_2010_1_31:154842002;;SNOMEDCT_2010_1_31:191124002;;SNOMEDCT_2010_1_31:191402006;;SNOMEDCT_2010_1_31:191446003;;SNOMEDCT_2010_1_31:267552000;;SNOMEDCT_2010_1_31:267573000;;SNOMEDCT_2010_1_31:34093004;;UMLS_CUI:C0018939 | ||
|is_a=DOID:1287 | |is_a=DOID:1287 | ||
|synonym="Blood disease" EXACT [SNOMEDCT_2005_07_31:154785002];;"blood disorder" EXACT [CSP2005:0427-3600];;"Blood dyscrasia NOS" EXACT [MTHICD9_2006:289.9];;"disease of hematopoietic system" EXACT [];;"DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS" EXACT [ICD9CM_2006:280-289.99];;"Hematological disease" EXACT [MTH:NOCODE] | |synonym="Blood disease" EXACT [SNOMEDCT_2005_07_31:154785002];;"blood disorder" EXACT [CSP2005:0427-3600];;"Blood dyscrasia NOS" EXACT [MTHICD9_2006:289.9];;"disease of hematopoietic system" EXACT [];;"DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS" EXACT [ICD9CM_2006:280-289.99];;"Hematological disease" EXACT [MTH:NOCODE] | ||
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|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo | |||
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Revision as of 14:01, 11 June 2012
Name: | hematopoietic system disease | |
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Namespace: | disease_ontology | |
Xrefs: |
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Synonyms: |
"Blood disease" EXACT [SNOMEDCT_2005_07_31:154785002] "blood disorder" EXACT [CSP2005:0427-3600] "Blood dyscrasia NOS" EXACT [MTHICD9_2006:289.9] "disease of hematopoietic system" EXACT [] "DISEASE OF THE BLOOD AND BLOOD-FORMING ORGANS" EXACT [ICD9CM_2006:280-289.99] "Hematological disease" EXACT [MTH:NOCODE] |
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:1287(cardiovascular system disease) |
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Children
is a: | FF:10772-110F7 (myelodysplastic syndrome cell line:SKM-1),DOID:2355 (anemia) |
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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)
- 10808-111A7 (hereditary spherocytic anemia cell line:WIL2-NS)
Mouse (Mus musculus)
- 10772-110F7 (myelodysplastic syndrome cell line:SKM-1)
- 10808-111A7 (hereditary spherocytic anemia cell line:WIL2-NS)
Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:74 (hematopoietic system disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data