DOID:2962
From FANTOM5_SSTAR
| Name: | Cockayne syndrome | ||
|---|---|---|---|
| Namespace: | disease_ontology | ||
| Definition: | "A monogenic disease that is caused by a rare autosomal recessive mutations in two DNA excision repair proteins, ERCC-8 and ERCC-6, and characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging." [url:http://en.wikipedia.org/wiki/Cockayne_syndrome, url:http://en.wikipedia.org/wiki/ERCC6, url:http://en.wikipedia.org/wiki/ERCC8, url:http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=216411] | ||
| Xrefs: |
| ||
| Synonyms: | "Cockayne's syndrome" RELATED [CSP2005:0977-5812] | ||
| Comments: | OMIM mapping confirmed by DO. [SN]. |
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:0050177(monogenic disease) |
|---|
Children
| is a: | FF:10583-108C7 () |
|---|
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:2962 (Cockayne syndrome), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data
No analysis results
