Dystrophy, dystrophia, muscular
- G71.00
- autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or BeckerG71.01
- benign (Becker type)G71.01
- benign (Becker type), scapuloperoneal with early contractures [Emery-Dreifuss]G71.09
- congenital (hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber)G71.09
- congenital (hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber), myotonicG71.11
- distalG71.09
- Duchenne typeG71.01
- Emery-DreifussG71.09
- Erb typeG71.02
- facioscapulohumeralG71.02
- Gower'sG71.01
- hereditary (progressive)G71.09
- Landouzy-Déjérine typeG71.02
- limb-girdleG71.039
- limb-girdle, alpha-sarcoglycan-relatedG71.0341
- limb-girdle, anoctamin-5-related autosomal recessive (R12)G71.035
- limb-girdle, autosomal recessive NECG71.038
- limb-girdle, beta-sarcoglycan-relatedG71.0342
- limb-girdle, calpain-3-relatedG71.032
- limb-girdle, calpain-3-related, autosomal dominantG71.031
- limb-girdle, calpain-3-related, autosomal recessiveG71.032
- limb-girdle, collagen VI related
- limb-girdle, collagen VI related, autosomal dominantG71.031
- limb-girdle, collagen VI related, autosomal recessiveG71.038
- limb-girdle, D1 (autosomal dominant)G71.031
- limb-girdle, D2 (autosomal dominant)G71.031
- limb-girdle, D3 (autosomal dominant)G71.031
- limb-girdle, D4 (autosomal dominant)G71.031
- limb-girdle, D5 (autosomal dominant)G71.031
- limb-girdle, delta-sarcoglycan-relatedG71.0349
- limb-girdle, due to
- limb-girdle, due to, alpha sarcoglycan dysfunctionG71.0341
- limb-girdle, due to, anoctamin-5 dysfunctionG71.035
- limb-girdle, due to, beta sarcoglycan dysfunctionG71.0342
- limb-girdle, due to, fukutin related protein dysfunctionG71.036
- limb-girdle, due to, sarcoglycan dysfunction, specified NECG71.0349
- limb-girdle, FKRP-related autosomal recessiveG71.038
- limb-girdle, gamma-sarcoglycan-relatedG71.0349
- limb-girdle, R1 (autosomal recessive)G71.032
- limb-girdle, R2 (autosomal recessive)G71.033
- limb-girdle, R3 (autosomal recessive)G71.0341
- limb-girdle, R4 (autosomal recessive)G71.0342
- limb-girdle, R5 (autosomal recessive)G71.0349
- limb-girdle, R6 (autosomal recessive)G71.0349
- limb-girdle, R7 (autosomal recessive)G71.038
- limb-girdle, R8 (autosomal recessive)G71.038
- limb-girdle, R9 (autosomal recessive)G71.036
- limb-girdle, R10 (autosomal recessive)G71.038
- limb-girdle, R11 (autosomal recessive)G71.038
- limb-girdle, R12 (autosomal recessive)G71.035
- limb-girdle, R13 (autosomal recessive)G71.038
- limb-girdle, R14 (autosomal recessive)G71.038
- limb-girdle, R15 (autosomal recessive)G71.038
- limb-girdle, R16 (autosomal recessive)G71.038
- limb-girdle, R17 (autosomal recessive)G71.038
- limb-girdle, R18 (autosomal recessive)G71.038
- limb-girdle, R19 (autosomal recessive)G71.038
- limb-girdle, R20 (autosomal recessive)G71.038
- limb-girdle, R21 (autosomal recessive)G71.038
- limb-girdle, R22 (autosomal recessive)G71.038
- limb-girdle, R23 (autosomal recessive)G71.038
- limb-girdle, R24 (autosomal recessive)G71.038
- limb-girdle, type 1 (autosomal dominant)G71.031
- limb-girdle, type 1A (autosomal dominant)G71.031
- limb-girdle, type 1B (autosomal dominant)G71.031
- limb-girdle, type 1C (autosomal dominant)G71.031
- limb-girdle, type 1E (autosomal dominant)G71.031
- limb-girdle, type 1H (autosomal dominant)G71.031
- limb-girdle, type 1I (autosomal dominant)G71.031
- limb-girdle, type 2 (autosomal recessive)G71.038
- limb-girdle, type 2 (autosomal recessive), specified NECG71.038
- limb-girdle, type 2A (autosomal recessive)G71.032
- limb-girdle, type 2B (autosomal recessive)G71.033
- limb-girdle, type 2C (autosomal recessive)G71.0349
- limb-girdle, type 2D (autosomal recessive)G71.0341
- limb-girdle, type 2E (autosomal recessive)G71.0342
- limb-girdle, type 2F (autosomal recessive)G71.0349
- limb-girdle, type 2G (autosomal recessive)G71.038
- limb-girdle, type 2H (autosomal recessive)G71.038
- limb-girdle, type 2I (autosomal recessive)G71.036
- limb-girdle, type 2J (autosomal recessive)G71.038
- limb-girdle, type 2K (autosomal recessive)G71.038
- limb-girdle, type 2L (autosomal recessive)G71.035
- limb-girdle, type 2M (autosomal recessive)G71.038
- limb-girdle, type 2N (autosomal recessive)G71.038
- limb-girdle, type 2O (autosomal recessive)G71.038
- limb-girdle, type 2P (autosomal recessive)G71.038
- limb-girdle, type 2Q (autosomal recessive)G71.038
- limb-girdle, type 2S (autosomal recessive)G71.038
- limb-girdle, type 2T (autosomal recessive)G71.038
- limb-girdle, type 2U (autosomal recessive)G71.038
- myotonicG71.11
- progressive (hereditary)G71.09
- progressive (hereditary), Charcot-Marie (-Tooth) typeG60.0
- pseudohypertrophic (infantile)G71.01
- scapulohumeralG71.02
- scapuloperonealG71.09
- severe (Duchenne type)G71.01
- specified type NECG71.09