Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare autosomal dominant distal hereditary motor neuropathy characterized by onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life. Sensory involvement is typically less pronounced or absent. The severity of the condition is variable, and both lower and upper extremities may be involved. Disease data Klasyfikacja Disease Synonimy Distal spinal muscular atrophy type 2 D dHMN2 dSMA2 dHMN2 dSMA2 Kod ORPHA 139525 Kod OMIM 615575 Kod ICD10 G12.2 Kod ICD11 8B61.4 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl