Term Name: Charcot-Marie-Tooth disease axonal type 2P
Synonyms: Charcot-Marie-Tooth disease type 2P, Charcot-Marie-Tooth neuropathy type 2P, CMT2P
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or heterozygous mutation in the LRSAM1 gene on chromosome 9q33.
Ontology: Human Disease [DOID:0110169]   ( DOID:0110169 )

Relationships
is a type of: autosomal dominant disease autosomal recessive disease Charcot-Marie-Tooth disease type 2