Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	Arthrogryposis multiplex congenita
ID	http://purl.bioontology.org/ontology/OMIM/MTHU009867
cui	C0003886
Manifestation of	http://purl.bioontology.org/ontology/OMIM/208085 http://purl.bioontology.org/ontology/OMIM/617468 http://purl.bioontology.org/ontology/OMIM/617301 http://purl.bioontology.org/ontology/OMIM/265000 http://purl.bioontology.org/ontology/OMIM/613404
notation	MTHU009867
prefLabel	Arthrogryposis multiplex congenita
tui	T047
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000029

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.bmicc.cn/ontology/ICD10CN/Q74.3	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/ICD10CM/Q74.3	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/ICD10CM/Q74.3	International Classification of Diseases, Version 10 - Clinical Modification	LOOM
http://purl.obolibrary.org/obo/DOID_0080954	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/ICD10/Q74.3	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/ICD10/Q74.3	International Classification of Diseases, Version 10	LOOM
http://purl.bioontology.org/ontology/MESH/D001176	Medical Subject Headings	CUI
http://purl.bmicc.cn/ontology/ICD11CN/LD26.41	International Classification of Diseases, 11th Edition, China	LOOM