disease has basis in disruption of disease caused by disruption of disease disrupts disease causes disruption of RNA binding regulation of RNA splicing progressive muscular dystrophy myotonic dystrophy https://github.com/monarch-initiative/mondo/issues/5658 https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/myotonic_disease https://www.malacards.org/card/myotonic_dystrophy icd11.foundation:192087511 OMIMPS:160900 NANDO:2200864 DOID:450 ICD10CM:G71.11 MEDGEN:10239 NANDO:1200495 GARD:0010419 Orphanet:206647 myotonia atrophica MedDRA:10068871 myotonia dystrophica UMLS:C0027126 MONDO:0016107 ICD9:359.2 An inherited progressive disorder affecting the muscles. It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies. myotonic disease inherited myotonic dystrophy MESH:D009223 SCTID:240104008 NCIT:C84914 myotonic syndrome