DOID:893

Name:	Wilson disease
Namespace:	disease_ontology
Xrefs:	links: MSH:D006527 NCI:C84756 OMIM:277900 SNOMEDCT_2010_1_31:154751003 SNOMEDCT_2010_1_31:190823004 SNOMEDCT_2010_1_31:191710006 SNOMEDCT_2010_1_31:192640001 SNOMEDCT_2010_1_31:267504005 SNOMEDCT_2010_1_31:88518009 UMLS_CUI:C0019202
Synonyms:	"Cerebral pseudosclerosis (disorder)" EXACT [SNOMEDCT_2005_07_31:192640001] "hepatolenticular degeneration" EXACT [] "Westphal pseudosclerosis" EXACT [CSP2005:1849-4349] "Westphal-Strumpell syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:190823004] "Wilson's disease" EXACT [SNOMEDCT_2005_07_31:267504005] "Wilson's disease" EXACT [SNOMEDCT_2005_07_31:154751003] "Wilson's disease" EXACT [MTHICD9_2006:275.1] "Wilson's disease (disorder)" EXACT [SNOMEDCT_2005_07_31:88518009] "Wilson's disease * (disorder)" EXACT [SNOMEDCT_2005_07_31:191710006]
Comments:	OMIM mapping confirmed by DO. [SN].

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:409(liver disease),DOID:896(metal metabolism disorder)

Children

is a:	FF:10578-108C2 (),FF:10579-108C3 (),FF:10582-108C6 ()

Ontology Tree: Loaded from BioPortal

Ontorolgy tree(Small window open)

FF samples

Human (Homo sapiens)

• 10578-108C2
• 10579-108C3
• 10582-108C6

Mouse (Mus musculus)

• 10578-108C2
• 10579-108C3
• 10582-108C6

Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:893 (Wilson disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data

---

No analysis results