DOID:3247
From FANTOM5_SSTAR
Name: | rhabdomyosarcoma | ||
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Namespace: | FANTOM | ||
Definition: | "A myosarcoma that arise from skeletal muscle progenitors." [url:http://en.wikipedia.org/wiki/Rhabdomyosarcoma] | ||
Xrefs: |
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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) |
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Children
is a: | FF:10734-110B5 () |
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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