ICD-10: G71.11

Myotonic muscular dystrophy

Clinical Information

Inclusion Terms

  • Dystrophia myotonica [Steinert]
  • Steinert disease
  • Myotonic dystrophy
  • Myotonia atrophica
  • Proximal myotonic myopathy (PROMM)

Related Diseases

Hirata disease monogenic disease obsolete physical disorder OBSOLETED TERM Danon disease Frasier syndrome obsolete acroosteolysis Gamstorp-Wohlfart syndrome posterior polar cataract Charcot-Marie-Tooth disease type 4 obsolete Majewski syndrome obsolete Verma-Naumoff syndrome glycogen storage disease XV ABCD syndrome ADULT syndrome anauxetic dysplasia 1 Bamforth-Lazarus syndrome Bart-Pumphrey syndrome Birk-Barel syndrome Bjornstad syndrome Brody myopathy variable age at onset electroclinical syndrome PSAT deficiency autosomal dominant disease Y-linked monogenic disease autosomal genetic disease Qazi Markouizos syndrome rapadilino syndrome Ogden syndrome Kahrizi syndrome Perrault syndrome IMAGe syndrome spastic ataxia 3 spinocerebellar ataxia type 20 thoracic disease Kennedy's disease homocarnosinosis amyotrophic lateral sclerosis type 21 Baraitser-Winter syndrome MASA syndrome Smith-McCort dysplasia rippling muscle disease 2 Ohdo syndrome Rapp-Hodgkin syndrome mitochondrial complex V (ATP synthase) deficiency nuclear type 2 CEDNIK syndrome acrorenal syndrome Stormorken syndrome Vici syndrome Galloway-Mowat syndrome 1 orofaciodigital syndrome IV orofaciodigital syndrome VII orofaciodigital syndrome XI chromosome 15q25 deletion syndrome chromosome 16q22 deletion syndrome chromosome 17p13.1 deletion syndrome chromosome 3q29 microdeletion syndrome chromosome 6q11-q14 deletion syndrome chromosome 5p13 duplication syndrome salt and pepper syndrome EAST syndrome Barber-Say syndrome 3MC syndrome 3 Yunis-Varon syndrome ulnar-mammary syndrome lethal congenital contracture syndrome 3 syndromic X-linked intellectual disability Lubs type MEHMO syndrome Prieto syndrome Wilson-Turner syndrome Miles-Carpenter syndrome Christianson syndrome myotonic dystrophy type 1

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