DOID:14447

Name:	gonadal dysgenesis
Namespace:	disease_ontology
Xrefs:	links: 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
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)

Children

is a:	DOID:3491 (Turner's syndrome)

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: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