Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024

Preferred Name	fibroblast growth factor receptor 2
Synonyms	CD332 TK25 CEK3 Pfeiffer syndrome Crouzon syndrome ECT1 TK14 K-SAM
ID	http://www.orpha.net/ORDO/Orphanet_132262
alternative_term	CD332 TK25 CEK3 Pfeiffer syndrome Crouzon syndrome ECT1 TK14 K-SAM
hasDbXref	IUPHAR:1809 Ensembl:ENSG00000066468 SwissProt:P21802 Genatlas:FGFR2 ClinVar:FGFR2 Reactome:P21802 OMIM:176943 HGNC:3689
label	fibroblast growth factor receptor 2
prefixIRI	ORDO:Orphanet_132262
prefLabel	fibroblast growth factor receptor 2
symbol	FGFR2
subClassOf	http://www.orpha.net/ORDO/Orphanet_410298

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/PR_000001449	OBA	LOOM
http://purl.obolibrary.org/obo/dinto_2717	DINTO	LOOM
http://purl.obolibrary.org/obo/PR_000001449	PR	LOOM
http://purl.obolibrary.org/obo/PR_000001449	INBANCIDO	LOOM
http://purl.obolibrary.org/obo/PR_000001449	GO-PLUS	LOOM
http://purl.obolibrary.org/obo/PR_000001449	CIDO	LOOM
http://purl.obolibrary.org/obo/PR_000001449	NIFSTD	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C17411	NCIT	LOOM
http://www.ncbi.nlm.nih.gov/gene/14183	NIFSTD	LOOM
http://purl.uniprot.org/uniprot/P21802	FTC	LOOM
http://www.limics.org/hrdo/rdfns#gen_id_16664	HRDO	LOOM
http://purl.org/skeletome/bonedysplasia#P000068	BDO	LOOM
http://purl.obolibrary.org/obo/NCIT_C17411	BERO	LOOM
http://www.drugtargetontology.org/dto/DTO_03100150	DTO	LOOM
http://purl.bioontology.org/ontology/OMIM/176943	OMIM	LOOM