Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation

Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation (disorder)

active

Code	`764730007`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20180731

Synonyms

Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation

Parents (1)

1156835005Autosomal dominant Charcot-Marie-Tooth disease type 2 disorder

Children (0)

None (leaf concept).