Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024

Preferred Name	Robinow-Sorauf syndrome
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_3106
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=3106
hasDbXref	MeSH:C537183 OMIM:180750 UMLS:C1867146
label	Robinow-Sorauf syndrome
notation	ORPHA:3106
prefixIRI	ORDO:Orphanet_3106
prefLabel	Robinow-Sorauf syndrome
reason_for_obsolescence	This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Saethre-Chotzen syndrome
subClassOf	http://www.orpha.net/ORDO/Orphanet_C044

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0008391	MONDO	LOOM
http://identifiers.org/omim/180750	REXO	LOOM
http://identifiers.org/omim/180750	GEXO	LOOM
http://identifiers.org/omim/180750	RETO	LOOM
http://purl.obolibrary.org/obo/OMIM_180750	CCO	LOOM
http://purl.bioontology.org/ontology/OMIM/180750	OMIM	LOOM
http://www.limics.org/hrdo/rdfns#pat_id_2780	HRDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0008391	DOVES	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C537183	RH-MESH	LOOM
http://purl.bioontology.org/ontology/MESH/C537183	MESH	LOOM