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DOID:1485

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Name:cystic fibrosis
Namespace:disease_ontology
Xrefs:
links:

ICD9CM:277.0
MSH:D003550
NCI:C2975
OMIM:219700
SNOMEDCT_2010_1_31:154767009
SNOMEDCT_2010_1_31:190905008
SNOMEDCT_2010_1_31:190911006
SNOMEDCT_2010_1_31:85809002

UMLS_CUI:C0010674
Synonyms: "CF" EXACT []
"mucoviscidosis" EXACT []
Comments:OMIM mapping confirmed by DO. [SN].
Alt_id: DOID:12447
DOID:13383
DOID:14395
DOID:1484

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:0050177(monogenic disease)



Children


is a:FF:10634-108I4 ()


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:1485 (cystic fibrosis), sorted by p-values
Analyst: Hideya Kawaji

link to source dataset
human : data
mouse : data


No analysis results