DO_rare_slim DO_FlyBase_slim hereditary sensory and autonomic neuropathy disease_ontology ORDO:140471 ICD10CM:G60.8 GARD:12688 MESH:D009477 DOID:0050548 SNOMEDCT_US_2025_09_01:128205005 ICD10CM:G60.8 UMLS_CUI:C0027889 GARD:12688 MIM:PS162400 A neuropathy characterized by axonal atrophy and degeneration, exclusively or predominantly affecting the sensory neurons, and variable autonomic dysfunction that has_material_basis_in an inherited mutation. Loss of pain and temperature sensation is an early and predominant, but not universal, symptom. MESH:D009477 MIM:PS162400 HSAN HSN UMLS_CUI:C0027889 ORDO:140471 hereditary sensory neuropathy neuropathy