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

Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation (disorder)

active

Code	`1187566006`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20220131

Synonyms

Autosomal dominant Charcot-Marie-Tooth disease type 2 due to trafficking from endoplasmic reticulum to golgi regulator mutation

Parents (1)

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

Children (0)

None (leaf concept).