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DOID:3491: Difference between revisions

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(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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|located_in=
|located_in=
|part_of=
|part_of=
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo
|is_obsolete=
|preceded_by=
}}
}}

Revision as of 14:00, 11 June 2012

Name:Turner's syndrome
Namespace:disease_ontology
Xrefs:
links:

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
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)



Children


is a:FF:10814-111B4 ()

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