Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	Pierre Robin syndrome
ID	http://purl.bioontology.org/ontology/OMIM/MTHU015092
cui	C0031900
Manifestation of	http://purl.bioontology.org/ontology/OMIM/192430
notation	MTHU015092
prefLabel	Pierre Robin syndrome
tui	T019
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000089

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C85010	National Cancer Institute Thesaurus	LOOM
http://purl.bioontology.org/ontology/MESH/D010855	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D010855	Medical Subject Headings	LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q87.0	International Classification of Diseases, Version 10 - Clinical Modification	CUI