Logical Observation Identifier Names and Codes

Last uploaded: March 1, 2019

Preferred Name	Congenital hypothyroidism
ID	http://purl.bioontology.org/ontology/LNC/LP56766-6
Component of	http://purl.bioontology.org/ontology/LNC/46763-9 http://purl.bioontology.org/ontology/LNC/57705-6 http://purl.bioontology.org/ontology/LNC/46762-1
cui	C0010308
notation	LP56766-6
prefLabel	Congenital hypothyroidism
tui	T047
subClassOf	http://purl.bioontology.org/ontology/LNC/LP56737-7

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/HP_0000851	Human Phenotype Ontology	LOOM
http://purl.bioontology.org/ontology/MESH/D003409	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D003409	Medical Subject Headings	LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU038801	Online Mendelian Inheritance in Man	CUI
http://purl.obolibrary.org/obo/DOID_0050328	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/ICD10CM/E03.1	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU003987	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU003987	Online Mendelian Inheritance in Man	LOOM
http://purl.bmicc.cn/ontology/ICD11CN/5A00.0	International Classification of Diseases, 11th Edition, China	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26734	National Cancer Institute Thesaurus	LOOM