G71
Details
-
androgen insensitivity syndrome (E34.5-)
-
congenital adrenal hyperplasia (E25.0)
-
hemolytic anemias attributable to enzyme disorders (D55.-)
-
Marfan’s syndrome (Q87.4)
-
5-alpha-reductase deficiency (E29.1)
- G71.0
Muscular dystrophy
- G71.00
Muscular dystrophy unspecified
- G71.01
Duchenne or Becker muscular dystrophy
- G71.02
Facioscapulohumeral muscular dystrophy
- G71.03
Limb girdle muscular dystrophies
- G71.031
Autosomal dominant limb girdle muscular dystrophy
- G71.032
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
- G71.033
Limb girdle muscular dystrophy due to dysferlin dysfunction
- G71.034
Limb girdle muscular dystrophy due to sarcoglycan dysfunction
- G71.0340
Limb girdle muscular dystrophy due to sarcoglycan dysfunction unspecified
- G71.0341
Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
- G71.0342
Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
- G71.0349
Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- G71.035
Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
- G71.038
Other limb girdle muscular dystrophy
- G71.039
Limb girdle muscular dystrophy, unspecified
- G71.09
Other specified muscular dystrophies
- G71.1
Myotonic disorders
- G71.11
Myotonic muscular dystrophy
- G71.12
Myotonia congenita
- G71.13
Myotonic chondrodystrophy
- G71.14
Drug induced myotonia
- G71.19
Other specified myotonic disorders
- G71.2
Congenital myopathies
- G71.20
Congenital myopathy, unspecified
- G71.21
Nemaline myopathy
- G71.22
Centronuclear myopathy
- G71.220
X-linked myotubular myopathy
- G71.228
Other centronuclear myopathy
- G71.29
Other congenital myopathy
- G71.3
Mitochondrial myopathy, not elsewhere classified
- G71.8
Other primary disorders of muscles
- G71.9
Primary disorder of muscle, unspecified