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DOID:893

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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
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.

link to ontology dataset
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

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:893 (Wilson disease), sorted by p-values
Analyst: Hideya Kawaji

link to source dataset
human : data
mouse : data


No analysis results