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DOID:1927: Difference between revisions

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Latest revision as of 16:32, 26 June 2012

Name:sphingolipidosis
Namespace:disease_ontology
Xrefs:
links:

MSH:D013106
SNOMEDCT_2010_1_31:238028008
SNOMEDCT_2010_1_31:58459009

UMLS_CUI:C0037899
Synonyms: "sphingolipidoses" EXACT []
"Sphingolipidosis (disorder)" EXACT [SNOMEDCT_2005_07_31:238028008]
"Sphingolipidosis, NOS" EXACT [SNOMEDCT_2005_07_31:58459009]

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:9455(lipid storage disease)



Children


is a:DOID:2368 (gangliosidosis)

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:1927 (sphingolipidosis), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data


No analysis results