DO_rare_slim has material basis in existence starts during autosomal dominant disease distal myopathy 3 MIM:610099 MPD3 disease_ontology ORDO:399086 A distal myopathy that is characterized by adult onset of slowly progressive distal muscular weakness and atrophy affecting the upper and lower limbs, leading to difficulties using the hands and walking difficulties and that has significant linkage to 2 distinct regions on chromosomes 8p22-q11 and 12q13-q22 and that has_material_basis_in heterozygous mutation in the HNRNPA1 gene on chromosome 12q13. DOID:0111189 distal muscular dystrophy 3 distal myopathy type 3 distal myopathy autosomal dominant inheritance Adult onset