Preferred Name

Robinow-Sorauf syndrome

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

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http://purl.bioontology.org/ontology/OMIM/180750 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/MESH/C537183 Medical Subject Headings / 医学主题词表 LOOM
http://purl.obolibrary.org/obo/MONDO_0008391 Mondo Disease Ontology / Mondo疾病本体 LOOM