DOID:14447: Difference between revisions
From FANTOM5_SSTAR
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|id=DOID:14447
|name=gonadal dysgenesis
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|is_a=DOID:0080014
|synonym="Gonadal dysgenesis" EXACT [SNOMEDCT_2005_07_31:268356004];;"Gonadal...") |
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|id=DOID:14447 | |id=DOID:14447 | ||
|name=gonadal dysgenesis | |name=gonadal dysgenesis | ||
|namespace= | |namespace=disease_ontology | ||
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|xref= | |xref=ICD9CM:758.6;;MSH:D006059;;NCI:C26900;;NCI:C61420;;SNOMEDCT_2010_1_31:157020008;;SNOMEDCT_2010_1_31:205681004;;SNOMEDCT_2010_1_31:205692003;;SNOMEDCT_2010_1_31:205695001;;SNOMEDCT_2010_1_31:268356004;;SNOMEDCT_2010_1_31:38804009;;UMLS_CUI:C0018051 | ||
|is_a=DOID:0080014 | |is_a=DOID:0080014 | ||
|synonym="Gonadal dysgenesis" EXACT [SNOMEDCT_2005_07_31:268356004];;"Gonadal dysgenesis" EXACT [ | |synonym="Gonadal dysgenesis" EXACT [SNOMEDCT_2005_07_31:268356004];;"Gonadal dysgenesis" EXACT [ICD9CM_2006:758.6];;"Gonadal dysgenesis" EXACT [SNOMEDCT_2005_07_31:157020008];;"gonadal dysgenesis" EXACT [CSP2005:1254-8447];;"Gonadal dysgenesis (disorder)" EXACT [SNOMEDCT_2005_07_31:205681004];;"Gonadal dysgenesis NOS" EXACT [SNOMEDCT_2005_07_31:205692003];;"Gonadal dysgenesis NOS (disorder)" EXACT [SNOMEDCT_2005_07_31:205695001];;"Gonadal dysgenesis syndrome" EXACT [SNOMEDCT_2005_07_31:38804009] | ||
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Latest revision as of 16:31, 26 June 2012
| Name: | gonadal dysgenesis | ||
|---|---|---|---|
| Namespace: | disease_ontology | ||
| Xrefs: |
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| Synonyms: |
"Gonadal dysgenesis" EXACT [SNOMEDCT_2005_07_31:268356004] "Gonadal dysgenesis" EXACT [ICD9CM_2006:758.6] "Gonadal dysgenesis" EXACT [SNOMEDCT_2005_07_31:157020008] "gonadal dysgenesis" EXACT [CSP2005:1254-8447] "Gonadal dysgenesis (disorder)" EXACT [SNOMEDCT_2005_07_31:205681004] "Gonadal dysgenesis NOS" EXACT [SNOMEDCT_2005_07_31:205692003] "Gonadal dysgenesis NOS (disorder)" EXACT [SNOMEDCT_2005_07_31:205695001] "Gonadal dysgenesis syndrome" EXACT [SNOMEDCT_2005_07_31:38804009] |
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:0080014(chromosomal disease) |
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Children
| is a: | DOID:3491 (Turner's syndrome) |
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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:14447 (gonadal dysgenesis), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data
No analysis results
