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DOID:2355

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Name:anemia
Namespace:FANTOM
Xrefs:
links:

ICD9CM:285.9
MSH:D000740
NCI:C2869
SNOMEDCT_2010_1_31:154786001
SNOMEDCT_2010_1_31:154812000
SNOMEDCT_2010_1_31:191277004
SNOMEDCT_2010_1_31:267531008
SNOMEDCT_2010_1_31:271737000
SNOMEDCT_2010_1_31:64593003

UMLS_CUI:C0002871

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:74(hematopoietic system disease)



Children


is a:FF:10808-111A7 (hereditary spherocytic anemia cell line:WIL2-NS)

Ontology Tree: Loaded from BioPortal

Ontorolgy tree(Small window open)

FF samples

Human (Homo sapiens)

  • 10808-111A7 (hereditary spherocytic anemia cell line:WIL2-NS)

Mouse (Mus musculus)

  • 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:2355 (anemia), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data