Skyscape Web Viewer : International Classification of Diseases : ICD10 Index

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[G71.01] - Duchenne or Becker muscular dystrophy
[G71.02] - Facioscapulohumeral muscular dystrophy
[G71.02]-Fascioscapulohumeral myopathy
[G71.02]-Landouzy-Déjérine dystrophy or facioscapulohumeral atrophy
[G71.02]-Pseudohypertrophic muscular dystrophy (Erb's)
[G71.02]-Scapulohumeral myopathy
[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]-Dysferlinopathy
[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 α 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]-Anoctaminopathy
[G71.035] - Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
[G71.036] - Limb girdle muscular dystrophy due to fukutin related protein dysfunction
[G71.038] - Other limb girdle muscular dystrophy
[G71.039] - Limb girdle muscular dystrophy, unspecified
[G71.09] - Other specified muscular dystrophies
[G71.09]-Pseudohypertrophy, muscle
[G71.1] - Myotonic disorders
[G71.11]-Batten-Steinert syndrome
[G71.11]-Curschmann (-Batten) (-Steinert) disease or syndrome
[G71.11] - Myotonic muscular dystrophy
[G71.11]-Steinert's disease
[G71.12] - Myotonia congenita
[G71.12]-Thomsen disease