Hereditary Insensitivity To Pain With Anhidrosis(Hereditary sensory and autonomic neuropathy type 4) Explore Disorder's Alias
An Autosomal recessive mode(s) within the Neuronal disorders category
Candidate Gene Information
An Autosomal recessive mode(s) within the Neuronal 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 | NTRK1/4914 | neurotrophic receptor tyrosine kinase 1 | 1q23.1 | Chr1, NC_000001.11 (156815750..156881850) |
66101 nt | 19 | 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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Clinical Symptoms & Disabilities