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 | |