Congenital Sensory Neuropathy With Selective Loss Of Small Myelinated Fibers(Hereditary sensory and autonomic neuropathy type 5) Explore Disorder's Alias
An Autosomal recessive mode(s) within the Neuromuscular disorders category
Candidate Gene Information
An Autosomal recessive mode(s) within the Neuromuscular disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | NGF/4803 | nerve growth factor | 1p13.2 | Chr1, NC_000001.11 (115285917..115338249, complement) |
52333 nt | 4 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | SCN11A/11280 | sodium voltage-gated channel alpha subunit 11 | 3p22.2 | Chr3, NC_000003.12 (38845764..39051944, complement) |
206181 nt | 35 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: Orphanet OMIM GARD GTR MedGen MalaCards EMBL-EBI OLS Monarch Initiative NORD | ||||||||
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