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DOID:1485: Difference between revisions

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Latest revision as of 16:31, 26 June 2012

Name:cystic fibrosis
Namespace:disease_ontology
Xrefs:
links:

ICD9CM:277.0
MSH:D003550
NCI:C2975
OMIM:219700
SNOMEDCT_2010_1_31:154767009
SNOMEDCT_2010_1_31:190905008
SNOMEDCT_2010_1_31:190911006
SNOMEDCT_2010_1_31:85809002

UMLS_CUI:C0010674
Synonyms: "CF" EXACT []
"mucoviscidosis" EXACT []
Comments:OMIM mapping confirmed by DO. [SN].
Alt_id: DOID:12447
DOID:13383
DOID:14395
DOID:1484

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:0050177(monogenic disease)



Children


is a:FF:10634-108I4 ()

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:1485 (cystic fibrosis), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data


No analysis results