| Disease Aliases (38) | Charcot-marie-tooth disease, type 3 Cmt3 Cmt4f Charcot marie tooth disease, type 3 Charcot-marie-tooth disease, demyelinating, type 4f Charcot-marie-tooth disease type 3 Dejerine-sottas neuropathy Dejerine-sottas syndrome Dsn Dss Dejerine sottas disease Dejerine sottas neuropathy Dejerine sottas syndrome Dejerine-sottas hypertrophic neuropathy Disease, dejerine-sottas Déjérine-sottas disease Hereditary motor and sensory neuropathy type iii Hmsn 3 Hmsn iii Hmsn type iii Hmsn type iiis Hmsn3 Hsmn iii Hereditary hypertrophic neuropathy Hereditary motor and sensory neuropathy 3 Hereditary motor and sensory neuropathy type 3 Hereditary motor and sensory neuropathy, type iii Hereditary sensory-motor neuropathy, type iii Hereditary, type iii, motor and sensory neuropathy Hypertrophic neuropathy of dejerine sottas Hypertrophic demyelinative neuropathy of infancy Hypertrophic hereditary neuropathy Hypertrophic neuropathy of dejerine-sottas Hypertrophic neuropathy of infancy Neuropathy, dejerine-sottas Progressive hypertrophic interstitial neuropathy Syndrome, dejerine-sottas |
Associated Genes (4) NCBI-RefSeq: PMP22 (Peripheral myelin protein 22) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: EGR2 (Early growth response 2) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: MPZ (Myelin protein zero) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: PRX (Periaxin) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Dejerine-Sottas disease | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |