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| Term | hereditary sensory and autonomic neuropathy type 5 | ID (Ontology) | DOID:0070145 (Human Disease) |
| Definition | A hereditary sensory neuropathy characterized by impaired pain and thermal perception in the extremities and selective reduction in small myelinated fibers that has_material_basis_in homozygous mutation in the NGF gene on chromosome 1p13. | ||
| Also Known As | "hereditary sensory and autonomic neuropathy type V" ; "HSAN5" | ||
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autosomal genetic disease |__autosomal recessive disease____ neuropathy | |__hereditary sensory neuropathy__| hereditary sensory and autonomic neuropathy type 5 |
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| Is a |
hereditary sensory neuropathy autosomal recessive disease |
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GARD:12328 MESH:D000699 MESH:D009477 MIM:608654 NCI:C156360 ORDO:608654 SNOMEDCT_US_2023_03_01:128206006 SNOMEDCT_US_2023_03_01:403605007 UMLS_CUI:C0002768 UMLS_CUI:C0020075 |
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