Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum
MONDO:0032903Also known as: AMCNACC, arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum, Zain Syndrome
1 clinical trial for this condition and its sub-types.
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Disease
(680)
Hereditary disease
(176)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Congenital limb malformation
(3)
Disease of genetic or genomic mechanism
(2)
Arthrogryposis multiplex congenita
(1)
Arthrogryposis syndrome
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)