Parent term(s)
spinal muscular atrophy
+
Term with siblings
childhood spinal muscular atrophy +
adult spinal muscular atrophy
autosomal dominant adult-onset proximal spinal muscular atrophy
autosomal dominant distal hereditary motor neuronopathy
+
autosomal recessive distal hereditary motor neuronopathy
+
Kennedy's disease
spinal muscular atrophy with lower extremity predominant
+
spinal muscular atrophy with progressive myoclonic epilepsy
spinal muscular atrophy, Jokela type
X-linked distal spinal muscular atrophy 3
X-linked spinal muscular atrophy 2
Child term(s)
intermediate spinal muscular atrophy
juvenile spinal muscular atrophy
spinal muscular atrophy type 0
Werdnig-Hoffmann disease
denotes an 'is-a' relationship