Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	Congenital hypothyroidism
ID	http://purl.bioontology.org/ontology/OMIM/MTHU003987
cui	C0010308
Manifestation of	http://purl.bioontology.org/ontology/OMIM/610199 http://purl.bioontology.org/ontology/OMIM/147920 http://purl.bioontology.org/ontology/OMIM/606519
notation	MTHU003987
prefLabel	Congenital hypothyroidism
tui	T047
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000131

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/HP_0000851	Human Phenotype Ontology	LOOM
http://purl.bioontology.org/ontology/LNC/LP56766-6	Logical Observation Identifier Names and Codes	CUI
http://purl.bioontology.org/ontology/LNC/LP56766-6	Logical Observation Identifier Names and Codes	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/LNC/MTHU025182	Logical Observation Identifier Names and Codes	CUI
http://purl.bioontology.org/ontology/LNC/MTHU025182	Logical Observation Identifier Names and Codes	LOOM
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.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