Arthrogryposis

A rare, non-progressive congenital disorder characterized by multiple joint contractures which are present at birth.

Identifiers: MONDO:0008779
Part of: Hereditary neurological disease Movement disorder
Also known as: Arthrogryposes, congenital multiple · congenital multiple Arthrogryposes · congenital multiple arthrogryposis

Subtypes

Disease	ID	Subtypes	Genes
Freeman-Sheldon syndrome	MONDO:0008675	1	MYH3
Boylan dew greco syndrome	MONDO:0022025
Congenital contractural arachnodactyly	MONDO:0007363		FBN2
Distal arthrogryposis Moore weaver type	MONDO:0022998
Massa casaer ceulemans syndrome	MONDO:0043123

Including projects on subtypes.

No projects yet.