Human Disease Ontology 123

Last uploaded: September 28, 2023
Preferred Name

arthrogryposis multiplex congenita

Definitions

A nervous system disease that is characterized by development of multiple joint contractures affecting two or more areas of the body prior to birth.

ID

http://purl.obolibrary.org/obo/DOID_0080954

database_cross_reference

OMIM:PS617468

GARD:777

definition

A nervous system disease that is characterized by development of multiple joint contractures affecting two or more areas of the body prior to birth.

disease has basis in

http://purl.obolibrary.org/obo/HP_0001197

has material basis in

http://purl.obolibrary.org/obo/GENO_0000148

has_obo_namespace

disease_ontology

id

DOID:0080954

in_subset

http://purl.obolibrary.org/obo/doid#DO_rare_slim

label

arthrogryposis multiplex congenita

notation

DOID:0080954

prefLabel

arthrogryposis multiplex congenita

subClassOf

http://purl.obolibrary.org/obo/DOID_0050737

http://purl.obolibrary.org/obo/DOID_863

http://purl.obolibrary.org/obo/DOID_0080015

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http://purl.bioontology.org/ontology/ICD10CM/Q74.3 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU009867 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/ICD10/Q74.3 International Classification of Diseases, Version 10 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/LD26.41 International Classification of Diseases, 11th Edition, China LOOM