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| Term | hereditary sensory neuropathy type 4 | ID (Ontology) | DOID:0070146 (Human Disease) |
| Definition | A hereditary sensory neuropathy characterized by insensitivity to pain and anhidrosis that has_material_basis_in homozygous or compound heterozygous mutation in the NTRK1 gene on chromosome 1q23. | ||
| Also Known As | "hereditary sensory neuropathy type IV" ; "insensitivity to pain, congenital, with anhidrosis" | ||
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autosomal genetic disease |__autosomal recessive disease____ neuropathy | |__hereditary sensory neuropathy__| hereditary sensory neuropathy type 4 |
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| Is a |
hereditary sensory neuropathy autosomal recessive disease |
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GARD:3006 MESH:D009477 MIM:256800 NCI:C118633 ORDO:642 SNOMEDCT_US_2023_03_01:62985007 UMLS_CUI:C0020074 |
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