Disease core ontology applied to Rare Diseases

Last uploaded: February 7, 2014

Preferred Name	HNF1 homeobox B
Synonyms	LFB3
ID	http://www.limics.org/hrdo/rdfns#gen_id_17228
altLabel	LFB3 transcription factor 2, hepatic; LF-B3; variant hepatic nuclear factor VHNF1 TCF2
geneSymbol	HNF1B
id_Ensembl	ENSG00000108753
id_Genatlas	HNF1B
id_HGNC	11630
id_MIM	189907
id_Reactome	P35680
id_SwissProt	P35680
prefixIRI	hrdo:gen_id_17228
prefLabel	HNF1 homeobox B
subClassOf	http://www.limics.org/hrdo/rdfns#gen_id_1

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://www.orpha.net/ORDO/Orphanet_158588	ORDO	LOOM
	http://purl.bioontology.org/ontology/OMIM/189907	OMIM	LOOM