Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome

Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder)

active

Code	`763312008`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20180731

Parents (5)

16784003Amino acid transport disorder disorder
85995004Autosomal recessive hereditary disorder disorder
85102008Cerebellar ataxia disorder
66091009Congenital disease disorder
763597000Hereditary ataxia disorder

Children (0)

None (leaf concept).