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DOID:3247: Difference between revisions

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{{DOID
{{DOID
|id=DOID:3247
|alt_id=
|name=rhabdomyosarcoma
|namespace=disease_ontology
|def="A myosarcoma that arise from skeletal muscle progenitors." [url:http://en.wikipedia.org/wiki/Rhabdomyosarcoma]
|xref=MSH:D012208;;NCI:C3359;;SNOMEDCT_2010_1_31:134166003;;SNOMEDCT_2010_1_31:302847003;;SNOMEDCT_2010_1_31:30924005;;UMLS_CUI:C0035412
|is_a=DOID:4043
|synonym="rhabdomyoblastoma" EXACT [CSP2005:2011-4200];;"rhabdomyosarcoma" EXACT [NCI2004_11_17:C3359];;"Rhabdomyosarcoma (disorder)" EXACT [SNOMEDCT_2005_07_31:302847003];;"Rhabdomyosarcoma NOS (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:134166003];;"Rhabdomyosarcoma, no subtype (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:30924005]
|comment=
|comment=
|alt_id=
|disjoint_from=
|union_of=
|created_by=
|created_by=
|obo_creation_date=
|def="A myosarcoma that arise from skeletal muscle progenitors." [url:http://en.wikipedia.org/wiki/Rhabdomyosarcoma]
|subset=
|derives_from=
|derives_from=
|develops_from=
|develops_from=
|disjoint_from=
|has_quality=
|has_quality=
|id=DOID:3247
|is_a=DOID:4043
|is_obsolete=
|located_in=
|located_in=
|name=rhabdomyosarcoma
|namespace=disease_ontology
|obo_creation_date=
|part_of=
|part_of=
|preceded_by=
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo
|is_obsolete=
|subset=
|preceded_by=
|synonym="rhabdomyoblastoma" EXACT [CSP2005:2011-4200];;"rhabdomyosarcoma" EXACT [NCI2004_11_17:C3359];;"Rhabdomyosarcoma (disorder)" EXACT [SNOMEDCT_2005_07_31:302847003];;"Rhabdomyosarcoma NOS (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:134166003];;"Rhabdomyosarcoma, no subtype (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:30924005]
|union_of=
|xref=MSH:D012208;;NCI:C3359;;SNOMEDCT_2010_1_31:134166003;;SNOMEDCT_2010_1_31:302847003;;SNOMEDCT_2010_1_31:30924005;;UMLS_CUI:C0035412
}}
}}

Revision as of 10:34, 12 September 2014

Name:rhabdomyosarcoma
Namespace:disease_ontology
Definition:"A myosarcoma that arise from skeletal muscle progenitors." [url:http://en.wikipedia.org/wiki/Rhabdomyosarcoma]
Xrefs:
links:

MSH:D012208
NCI:C3359
SNOMEDCT_2010_1_31:134166003
SNOMEDCT_2010_1_31:302847003
SNOMEDCT_2010_1_31:30924005

UMLS_CUI:C0035412
Synonyms: "rhabdomyoblastoma" EXACT [CSP2005:2011-4200]
"rhabdomyosarcoma" EXACT [NCI2004_11_17:C3359]
"Rhabdomyosarcoma (disorder)" EXACT [SNOMEDCT_2005_07_31:302847003]
"Rhabdomyosarcoma NOS (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:134166003]
"Rhabdomyosarcoma, no subtype (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:30924005]

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:4043(skeletal muscle cancer)



Children


is a:FF:10734-110B5 ()

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:3247 (rhabdomyosarcoma), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data


No analysis results