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DOID:0050737

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Name:autosomal recessive disease
Namespace:FANTOM
Definition:{{{def}}}
Xrefs:
links:
{{{xref}}}:[1]
Synonyms: {{{synonym}}}
Comments:{{{comment}}}
Alt_id: {{{alt_id}}}
Subset: {{{subset}}}
Created by:{{{created_by}}}
Creation date:{{{obo_creation_date}}}
Has quality:{{{has_quality}}}

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:0050739(autosomal genetic disease)
disjoint_from:[[{{{disjoint_from}}}]]()
union_of:[[{{{union_of}}}]]()
derives_from:[[{{{derives_from}}}]]()
develops_from:[[{{{develops_from}}}]]()
has_quality:[[{{{has_quality}}}]]()
located_in:[[{{{located_in}}}]]()
part_of:[[{{{part_of}}}]]()



Children


is a:DOID:0050427 (xeroderma pigmentosum)

Ontology Tree: Loaded from BioPortal

Ontorolgy tree(Small window open)

FF samples

Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:0050737 (autosomal recessive disease), sorted by p-values
Analyst: Hideya Kawaji

link to source dataset
human : data
mouse : data


No analysis results







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