DOID:3491

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)

• 10814-111B4

Mouse (Mus musculus)

• 10814-111B4

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