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DOID:74

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Name:hematopoietic system disease
Namespace:FANTOM
Xrefs:
links:

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
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:2914(immune system disease)



Children


is a:FF:10772-110F7 (myelodysplastic syndrome cell line:SKM-1),DOID:2355 (anemia)

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