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)
Muscular dystrophy
Muscular dystrophy unspecified
Duchenne or Becker muscular dystrophy
Facioscapulohumeral muscular dystrophy
Limb girdle muscular dystrophies
Autosomal dominant limb girdle muscular dystrophy
Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
Limb girdle muscular dystrophy due to dysferlin dysfunction
Limb girdle muscular dystrophy due to sarcoglycan dysfunction
Limb girdle muscular dystrophy due to sarcoglycan dysfunction unspecified
Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
Other limb girdle muscular dystrophy
Limb girdle muscular dystrophy, unspecified
Other specified muscular dystrophies
Myotonic disorders
Myotonic muscular dystrophy
Myotonia congenita
Myotonic chondrodystrophy
Drug induced myotonia
Other specified myotonic disorders
Congenital myopathies
Congenital myopathy, unspecified
Nemaline myopathy
Centronuclear myopathy
X-linked myotubular myopathy
Other centronuclear myopathy
Other congenital myopathy
Mitochondrial myopathy, not elsewhere classified
Other primary disorders of muscles
Primary disorder of muscle, unspecified