Personal tools

DOID:11983

From FANTOM5_SSTAR

Jump to: navigation, search

Name:Prader-Willi syndrome
Namespace:disease_ontology
Xrefs:
links:

ICD9CM:759.81
MSH:D011218
NCI:C75463
OMIM:176270
SNOMEDCT_2010_1_31:205794007
SNOMEDCT_2010_1_31:89392001

UMLS_CUI:C0032897
Synonyms: "Prader - Willi syndrome" EXACT [SNOMEDCT_2005_07_31:205794007]
"Prader Willi syndrome" EXACT [CSP2005:1849-7731]
"Prader-Willi syndrome" EXACT [ICD9CM_2006:759.81]
"Prader-Willi syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:89392001]
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:0080014(chromosomal disease)



Children


is a:FF:10521-107E8 ()


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:11983 (Prader-Willi syndrome), sorted by p-values
Analyst: Hideya Kawaji

link to source dataset
human : data
mouse : data


No analysis results