Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 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 Classification Disease Synonyms Distal spinal muscular atrophy type 2 D dHMN2 dSMA2 dHMN2 dSMA2 ORPHA code 139525 OMIM code 615575 ICD10 code G12.2 ICD11 code 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