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Up to: Hereditary disease · Muscle tissue disorder · Arthrogryposis syndrome

Distal arthrogryposis

A muscle tissue disease characterized by congenital joint contractures of hand and feet.

0 trials tagged with this condition →

Freeman-Sheldon syndrome 1 trial Sub-types →
Congenital contractural arachnodactyly 1 trial
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A 1 trial
ACTC1-related distal arthrogryposis with congenital heart disease 0 trials
Ehlers-Danlos syndrome, musculocontractural type 0 trials Sub-types →
Gordon syndrome 0 trials
Sheldon-hall syndrome 0 trials Sub-types →
Arthrogryposis, distal, IIa 11 0 trials
Arthrogryposis, distal, type 12 0 trials
Arthrogryposis, distal, type 1C 0 trials
Arthrogryposis, distal, type 2B4 0 trials
Arthrogryposis, distal, type 2E 0 trials
Arthrogryposis, distal, with impaired proprioception and touch 0 trials
Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome 0 trials
Arthrogryposis-ectodermal dysplasia-other anomalies syndrome 0 trials
Arthrogryposis-like hand anomaly-sensorineural deafness syndrome 0 trials
Arthrogryposis-severe scoliosis syndrome 0 trials
Autism spectrum disorder - epilepsy - arthrogryposis syndrome 0 trials
Digitotalar dysmorphism 0 trials Sub-types →
Distal arthrogryposis Moore weaver type 0 trials
Distal arthrogryposis type 10 0 trials
Distal arthrogryposis type 5D 0 trials
Trismus-pseudocamptodactyly syndrome 0 trials