International Classification of Diseases, Version 10 - Clinical Modification - Congenital hypothyroidism without goiter - Classes

Last uploaded: January 29, 2019

Preferred Name	Congenital hypothyroidism without goiter
Synonyms	Congenital hypothyroidism NOS
ID	http://purl.bioontology.org/ontology/ICD10CM/E03.1
altLabel	Congenital hypothyroidism NOS Aplasia of thyroid (with myxedema) Congenital atrophy of thyroid
cui	C0749420 C0010308 C0342151 C0342154
Inverse of SIB	http://purl.bioontology.org/ontology/ICD10CM/E03.2 http://purl.bioontology.org/ontology/ICD10CM/E03.5 http://purl.bioontology.org/ontology/ICD10CM/E03.0 http://purl.bioontology.org/ontology/ICD10CM/E03.4 http://purl.bioontology.org/ontology/ICD10CM/E03.9 http://purl.bioontology.org/ontology/ICD10CM/E03.3 http://purl.bioontology.org/ontology/ICD10CM/E03.8
notation	E03.1
Order number	03664
prefLabel	Congenital hypothyroidism without goiter
tui	T019 T047
subClassOf	http://purl.bioontology.org/ontology/ICD10CM/E03

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.bmicc.cn/ontology/ICD10CN/E03.1	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/LNC/LP56766-6	Logical Observation Identifier Names and Codes	CUI
http://purl.bioontology.org/ontology/MESH/D003409	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU038801	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/LNC/MTHU025182	Logical Observation Identifier Names and Codes	CUI
http://purl.bioontology.org/ontology/OMIM/218700	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU003987	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/MESH/D050033	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/ICD10/E03.1	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU053628	Online Mendelian Inheritance in Man	CUI