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Human Disease

Charcot-Marie-Tooth disease, axonal type 2W

Term ID
DOID:0110162
Synonyms
  • autosomal dominant axonal Charcot-Marie-Tooth disease type 2W
  • Charcot-Marie-Tooth neuropathy type 2W
  • CMT2W
Definition
A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the HARS gene on chromosome 5q31. https://www.ncbi.nlm.nih.gov/pubmed/22930593
References
Ontology
Human Disease   ( DOID:0110162 )
Relationships
is a type of
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Genes Involved
Zebrafish Models