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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<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)

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 <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data


No analysis results