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