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DOID:5679

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Name:retinal disease
Namespace:disease_ontology
Xrefs:
links:

ICD9CM:362.9
MSH:D012164
NCI:C26875
NCI:C62601
SNOMEDCT_2010_1_31:193430004
SNOMEDCT_2010_1_31:267715002
SNOMEDCT_2010_1_31:29555009
SNOMEDCT_2010_1_31:35426003
SNOMEDCT_2010_1_31:399625000

UMLS_CUI:C0035309
Synonyms: "retina disorder" EXACT [CSP2005:1114-9311]
"Retinal disorder" EXACT [NCI2004_11_17:C26875]
"Retinopathy (disorder)" EXACT [SNOMEDCT_2005_07_31:399625000]

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:5614(eye disease)



Children


is a:DOID:4645 (retinal cancer)

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:5679 (retinal disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data


No analysis results