Arthrogryposis

Persistent flexure or contracture of a joint.

Also Known As:

Arthrogryposis Multiplex Congenita; Arthrogryposis Multiplex Congenita (AMC); Congenital Arthromyodysplasia; Congenital Multiple Arthrogryposis; Fibrous Ankylosis of Multiple Joints; Guérin-Stern Syndrome; Otto Syndrome; Rocher-Sheldon Syndrome; Rossi Syndrome; Arthrogryposes; Arthrogryposes, Congenital Multiple; Arthrogryposis Multiplex Congenitas; Arthrogryposis Multiplex Congenitas (AMC); Arthrogryposis, Congenital Multiple; Arthromyodysplasias, Congenital; Congenita, Arthrogryposis Multiplex; Congenita, Arthrogryposis Multiplex (AMC); Congenital Arthromyodysplasias; Congenital Multiple Arthrogryposes; Congenitas, Arthrogryposis Multiplex; Congenitas, Arthrogryposis Multiplex (AMC); Guerin Stern Syndrome; Guérin Stern Syndrome; Multiple Arthrogryposes, Congenital; Multiple Arthrogryposis, Congenital; Multiplex Congenita, Arthrogryposis; Multiplex Congenita, Arthrogryposis (AMC); Multiplex Congenitas, Arthrogryposis; Multiplex Congenitas, Arthrogryposis (AMC); Rocher Sheldon Syndrome; Syndrome, Guerin-Stern; Syndrome, Guérin-Stern; Syndrome, Otto; Syndrome, Rocher-Sheldon; Syndrome, Rossi; Amyoplasia Congenita; Arthromyodysplasia, Congenital; Guerin-Stern Syndrome; Myodystrophia Fetalis Deformans

Musculoskeletal Diseases: 719
- Muscular Diseases: 10128
  - Arthrogryposis: 324
- Joint Diseases: 6509
  - Arthrogryposis: 324
- Musculoskeletal Abnormalities: 43
  - Arthrogryposis: 324
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Musculoskeletal Abnormalities: 43
    - Arthrogryposis: 324

Spranger Schinzel Myers syndrome

Disease Context: Research Results