GenTIGSA Gene Database on Rare Genetic Disorders
Charcot-Marie-Tooth Disease, Type IA  
Disease Aliases (14)

Autosomal dominant charcot-marie-tooth disease with focally folded myelin sheaths type 1a

Charcot-marie-tooth disease type 1a

Charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1a

Charcot-marie-tooth disease, demyelinating, type 1a

Charcot-marie-tooth disease, type 1a

Charcot-marie-tooth neuropathy type 1a

Charcot-marie-tooth neuropathy, type 1a

Charcot-marie-tooth syndrome type 1a

Cmt 1a

Cmt1a

Hereditary motor and sensory neuropathy 1a

Hereditary motor and sensory neuropathy ia

Hmsn 1a

Hmsn1a

Associated Genes (0)
 

Cross-references of Charcot-Marie-Tooth disease, type IA OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations