DO_rare_slim has material basis in has symptom autosomal dominant disease hereditary neuropathy with liability to pressure palsies MESH:C536965 disease_ontology ORDO:640 UMLS_CUI:C0393814 DOID:0060843 SNOMEDCT_US_2025_09_01:230558006 MIM:162500 A neuropathy characterized by autosomal dominant inheritance of peroneal muscle weakness, peripheral neuropathy, hyporeflexia, tomacula, segmental demyelination/remyelination, decreased motor nerve conduction that has_material_basis_in deletion or point mutation of the PMP22 gene on chromosome 17p12. HNPP current pressure-sensitive neuropathy familial recurrent polyneuropathy heterozygous microdeletion 17p11.2p12 potato-grubbing palsy tomaculous neuropathy tulip-bulb digger's palsy neuropathy autosomal dominant inheritance muscle weakness