has material basis in germline mutation in disease has feature LMNA Dilated cardiomyopathy autosomal dominant disease heart-hand syndrome, Slovenian type https://rarediseases.info.nih.gov/diseases/9846/heart-hand-syndrome-slovenian-type https://www.malacards.org/card/heart_hand_syndrome_slovenian_type OMIM:610140 MEDGEN:341859 icd11.foundation:1814304618 UMLS:C1857829 GARD:0009846 Cardiac conduction disease-dilated cardiomyopathy-brachydactyly syndrome A rare autosomal dominant form of heart-hand syndrome, first described in members of a Slovenian family, that is characterized by adult onset, progressive cardiac conduction disease, tachyarrhythmias that can lead to sudden death, dilated cardiomyopathy and brachydactyly, with the hands less severely affected than the feet. Muscle weakness and/or myopathic electromyographic findings have been observed in some cases. MONDO:0012417 Orphanet:168796 MESH:C535852 SCTID:721014007 atriodigital dysplasia, Slovenian type heart-hand syndrome, Slovenian type obsolete syndrome associated with dilated cardiomyopathy heart-hand syndrome