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DOID:14447

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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
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:DOID:3491 (Turner's syndrome)

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:14447 (gonadal dysgenesis), sorted by p-values
Analyst: Hideya Kawaji

link to source dataset
human : data
mouse : data


No analysis results