G71.11 – Myotonic muscular dystrophy
Coding Notes
Active
Billable, valid for HIPAA-covered transactions
Applicable To
Dystrophia myotonica [Steinert]
Myotonia atrophica
Myotonic dystrophy
Proximal myotonic myopathy (PROMM)
Steinert disease
GEM Conversion to ICD-9 CM
Fs: 00000
–
Myotonic muscular dystrophy
MDC / MS-DRG Reference
Back Reference of Diagnostic Codes
Atrophy, atrophic
(of)
muscle, muscular
(diffuse) (general) (idiopathic) (primary)
M62.50
Cardiomyopathy
(familial) (idiopathic)
I42.9
due to
Curschmann disease or syndrome
(-Batten) (-Steinert)
G71.11
Disease, diseased
See also Syndrome
Dystrophy, dystrophia
congenital
(hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber)
G71.09
Myocardiopathy
(congestive) (constrictive) (familial) (hypertrophic nonobstructive) (idiopathic) (infiltrative) (obstructive) (primary) (restrictive) (sporadic)
See also Cardiomyopathy
I42.9
in
(due to)
mytonic, proximal
(PROMM)
G71.11
proximal myotonic
(PROMM)
G71.11
Syndrome
See also Disease
Curschmann
(-Batten) (-Steinert)
G71.11
Sibling Codes
Parent Sibling Codes
View in Tabular
Code | Title |
---|---|
G00-G99 | Diseases of the nervous system (G00-G99) |
G70-G73 | Diseases of myoneural junction and muscle (G70-G73) |
G71 | Primary disorders of muscles |
G71.1 | Myotonic disorders |
G71.11 |
Myotonic muscular dystrophy
Applicable to
Dystrophia myotonica [Steinert]
Myotonia atrophica
Myotonic dystrophy
Proximal myotonic myopathy (PROMM)
Steinert disease
|