DOID:3491
From FANTOM5_SSTAR
| Name: | Turner's syndrome |
|---|---|
| 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] |
| 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
