Orphanet Rare Disease Ontology

Last uploaded: December 4, 2024

Preferred Name	noggin
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_123854
hasDbXref	Ensembl:ENSG00000183691 SwissProt:Q13253 Reactome:Q13253 Genatlas:NOG OMIM:602991 ClinVar:NOG HGNC:7866
label	noggin
prefixIRI	ORDO:Orphanet_123854
prefLabel	noggin
symbol	NOG
subClassOf	http://www.orpha.net/ORDO/Orphanet_410298

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/RXNORM/1858663	RXNORM	LOOM
http://www.ncbi.nlm.nih.gov/gene/18121	NIFSTD	LOOM
http://purl.jp/bio/4/id/200906037570218830	IOBC	LOOM
http://purl.obolibrary.org/obo/PR_000000021	PR	LOOM
http://purl.obolibrary.org/obo/PR_000000021	NIFSTD	LOOM
http://www.semanticweb.org/cjf/ontologies/2022/8/NeuralReprogrammingOntology(NRO)#Noggin	NRO	LOOM
http://www.limics.org/hrdo/rdfns#gen_id_16557	HRDO	LOOM
http://purl.bioontology.org/ontology/OMIM/602991	OMIM	LOOM
http://purl.org/skeletome/bonedysplasia#P000132	BDO	LOOM