Severe early-onset axonal neuropathy due to mitofusin 2 deficiency

Severe early-onset axonal neuropathy due to mitofusin 2 deficiency (disorder)

active

Code	`766977007`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20180731

Synonyms

Autosomal recessive Charcot-Marie-Tooth disease Ouvrier type
Severe early-onset axonal neuropathy due to MFN2 (mitofusin 2) deficiency
Severe early-onset axonal neuropathy due to MFN2 deficiency

Parents (2)

85995004Autosomal recessive hereditary disorder disorder
398100001Hereditary motor and sensory neuropathy disorder

Children (0)

None (leaf concept).