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DOID:3149

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Name:keratoacanthoma
Namespace:disease_ontology
Xrefs:
links:

MSH:D007636
NCI:C3146
SNOMEDCT_2010_1_31:156395005
SNOMEDCT_2010_1_31:201061007
SNOMEDCT_2010_1_31:201064004
SNOMEDCT_2010_1_31:254662007
SNOMEDCT_2010_1_31:267858008
SNOMEDCT_2010_1_31:58220003

UMLS_CUI:C0022572
Synonyms: "keratoacanthoma" EXACT [CSP2005:2020-2121]
"keratoacanthoma" EXACT [MTH:NOCODE]
"Keratoacanthoma (disorder)" EXACT [SNOMEDCT_2005_07_31:254662007]
"Keratoacanthoma (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:58220003]

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:3151(skin squamous cell carcinoma)



Children


is a:FF:10713-109I2 (),FF:10791-110H8 (keratoacanthoma cell line:HKA-1)

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:3149 (keratoacanthoma), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data