DOID:3491: Difference between revisions
From FANTOM5_SSTAR
(Created page with "{{DOID
|id=DOID:3491
|name=Turner's syndrome
|namespace=
|def=
|xref=
|is_a=DOID:14447
|synonym="Bonnevie-Ullrich syndrome" EXACT [SNOMEDCT_2005_07_31:38804009];;"Bonne...") |
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|id=DOID:3491 | |id=DOID:3491 | ||
|name=Turner's syndrome | |name=Turner's syndrome | ||
|namespace= | |namespace=disease_ontology | ||
|def= | |def= | ||
|xref= | |xref=MSH:C531840;;MSH:D014424;;NCI:C26900;;NCI:C36630;;NCI:C85210;;SNOMEDCT_2010_1_31:157020008;;SNOMEDCT_2010_1_31:205685008;;SNOMEDCT_2010_1_31:205691005;;SNOMEDCT_2010_1_31:254279009;;SNOMEDCT_2010_1_31:268299006;;SNOMEDCT_2010_1_31:268356004;;SNOMEDCT_2010_1_31:38804009;;UMLS_CUI:C0041408;;UMLS_CUI:C1527168 | ||
|is_a=DOID:14447 | |is_a=DOID:14447 | ||
|synonym="Bonnevie-Ullrich syndrome" EXACT [SNOMEDCT_2005_07_31:38804009];;"Bonnevie-Ullrich syndrome NOS" EXACT [SNOMEDCT_2005_07_31:205691005];;"Bonnevie-Ullrich syndrome NOS (disorder)" EXACT [SNOMEDCT_2005_07_31:254279009];;"Gonadal dysgenesis - Turner" EXACT [SNOMEDCT_2005_07_31:268356004];;"Gonadal dysgenesis - Turner" EXACT [SNOMEDCT_2005_07_31:157020008];;"Karyotype 45, X" EXACT [SNOMEDCT_2005_07_31:205685008];;"Monosomy X" EXACT [NCI2004_11_17:C36630];;"monosomy X syndrome" EXACT [CSP2005:1254-8447];;"Turner syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:38804009];;"Turner's syndrome NOS" EXACT [SNOMEDCT_2005_07_31:205691005];;"Turner's syndrome NOS (disorder)" EXACT [SNOMEDCT_2005_07_31:268299006];;"XO syndrome" EXACT [MTHICD9_2006:758.6] | |synonym="Bonnevie-Ullrich syndrome" EXACT [SNOMEDCT_2005_07_31:38804009];;"Bonnevie-Ullrich syndrome NOS" EXACT [SNOMEDCT_2005_07_31:205691005];;"Bonnevie-Ullrich syndrome NOS (disorder)" EXACT [SNOMEDCT_2005_07_31:254279009];;"Gonadal dysgenesis - Turner" EXACT [SNOMEDCT_2005_07_31:268356004];;"Gonadal dysgenesis - Turner" EXACT [SNOMEDCT_2005_07_31:157020008];;"Karyotype 45, X" EXACT [SNOMEDCT_2005_07_31:205685008];;"Monosomy X" EXACT [NCI2004_11_17:C36630];;"monosomy X syndrome" EXACT [CSP2005:1254-8447];;"Turner syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:38804009];;"Turner's syndrome NOS" EXACT [SNOMEDCT_2005_07_31:205691005];;"Turner's syndrome NOS (disorder)" EXACT [SNOMEDCT_2005_07_31:268299006];;"XO syndrome" EXACT [MTHICD9_2006:758.6] | ||
|comment= | |comment=No OMIM mapping, confirmed by DO. [LS]. | ||
|alt_id=DOID:5448 | |alt_id=DOID:5448 | ||
|disjoint_from= | |disjoint_from= | ||
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|subset= | |subset= | ||
|derives_from= | |derives_from= | ||
|develops_from= | |develops_from= | ||
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|located_in= | |located_in= | ||
|part_of= | |part_of= | ||
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo | |||
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Latest revision as of 16:32, 26 June 2012
| Name: | Turner's syndrome | ||
|---|---|---|---|
| Namespace: | disease_ontology | ||
| Xrefs: |
| ||
| Synonyms: |
"Bonnevie-Ullrich syndrome" EXACT [SNOMEDCT_2005_07_31:38804009] "Bonnevie-Ullrich syndrome NOS" EXACT [SNOMEDCT_2005_07_31:205691005] "Bonnevie-Ullrich syndrome NOS (disorder)" EXACT [SNOMEDCT_2005_07_31:254279009] "Gonadal dysgenesis - Turner" EXACT [SNOMEDCT_2005_07_31:268356004] "Gonadal dysgenesis - Turner" EXACT [SNOMEDCT_2005_07_31:157020008] "Karyotype 45, X" EXACT [SNOMEDCT_2005_07_31:205685008] "Monosomy X" EXACT [NCI2004_11_17:C36630] "monosomy X syndrome" EXACT [CSP2005:1254-8447] "Turner syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:38804009] "Turner's syndrome NOS" EXACT [SNOMEDCT_2005_07_31:205691005] "Turner's syndrome NOS (disorder)" EXACT [SNOMEDCT_2005_07_31:268299006] "XO syndrome" EXACT [MTHICD9_2006:758.6] | ||
| Comments: | No OMIM mapping, confirmed by DO. [LS]. | ||
| Alt_id: | DOID:5448 |
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:14447(gonadal dysgenesis) |
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Children
| is a: | FF:10814-111B4 () |
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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:3491 (Turner's syndrome), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data
No analysis results
