| Disease Aliases (21) | Charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1a Charcot-marie-tooth neuropathy, type 1a Cmt 1a Cmt1a Charcot marie tooth disease, type 1a Charcot marie tooth disease, type ia Charcot marie tooth neuropathy, type 1a Charcot marie tooth disease type 1a Charcot-marie-tooth disease, type 1a Charcot-marie-tooth disease, type ia Charcot-marie-tooth disease type 1a Charcot-marie-tooth disease, demyelinating, type 1a Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Charcot-marie-tooth neuropathy type 1a Hereditary motor and sensory neuropathy ia Hmsn 1a Hmsn ia Hmsn1a Hereditary motor and sensory neuropathy 1a Microduplication 17p12 Autosomal dominant charcot-marie-tooth disease with focally folded myelin sheaths type 1a |
Associated Genes (1) NCBI-RefSeq: PMP22 (Peripheral myelin protein 22) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Charcot-Marie-Tooth disease, type IA | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |