International Classification of Diseases, Version 10 - Clinical Modification - Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] - Classes

Last uploaded: January 29, 2019

Preferred Name	Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
ID	http://purl.bioontology.org/ontology/ICD10CM/G12.0
cui	C0043116
Inverse of SIB	http://purl.bioontology.org/ontology/ICD10CM/G12.8 http://purl.bioontology.org/ontology/ICD10CM/G12.2 http://purl.bioontology.org/ontology/ICD10CM/G12.9 http://purl.bioontology.org/ontology/ICD10CM/G12.1
notation	G12.0
Order number	05831
prefLabel	Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
tui	T047
subClassOf	http://purl.bioontology.org/ontology/ICD10CM/G12

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/OMIM/600354	Online Mendelian Inheritance in Man	CUI
http://purl.bmicc.cn/ontology/ICD10CN/G12.0	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/MESH/D014897	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/OMIM/253300	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/ICD10/G12.0	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/ICD10/G12.0	International Classification of Diseases, Version 10	LOOM