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Dystrophy, dystrophia
    adiposogenital E23.6
    autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker G71.01
    Becker's type G71.01
    cervical sympathetic G90.2
    choroid (hereditary) H31.20
        central areolar H31.22
        choroideremia H31.21
        gyrate atrophy H31.23
        specified type NEC H31.29
    cornea (hereditary) H18.50
        endothelial H18.51
        epithelial H18.52
        granular H18.53
        lattice H18.54
        macular H18.55
        specified type NEC H18.59
    Duchenne's type G71.01
    due to malnutrition E45
    Erb's G71.02
    Fuchs' H18.51
    Gower's muscular G71.01
    hair L67.8
    infantile neuraxonal G31.89
    Landouzy-Déjérine G71.02
    Leyden-Möbius G71.09
    muscular G71.00
        autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker G71.01
        benign (Becker type) G71.01
            scapuloperoneal with early contractures [Emery-Dreifuss] G71.09
        congenital (hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber) G71.09
            myotonic G71.11
        distal G71.09
        Duchenne type G71.01
        Emery-Dreifuss G71.09
        Erb type G71.02
        facioscapulohumeral G71.02
        Gower's G71.01
        hereditary (progressive) G71.09
        Landouzy-Déjérine type G71.02
        limb-girdle G71.09
        myotonic G71.11
        progressive (hereditary) G71.09
            Charcot-Marie type (-Tooth) G60.0
        pseudohypertrophic (infantile) G71.01
        scapulohumeral G71.02
        scapuloperoneal G71.09
        severe (Duchenne type) G71.01
        specified type NEC G71.09
    myocardium, myocardial --see Degeneration, myocardial
    myotonic, myotonica G71.11
    nail L60.3
        congenital Q84.6
    nutritional E45
    ocular G71.09
    oculocerebrorenal E72.03
    oculopharyngeal G71.09
    ovarian N83.8
    polyglandular E31.8
    reflex (neuromuscular) (sympathetic) --see Syndrome, pain, complex regional I
    retinal (hereditary) H35.50
        in
            lipid storage disorders E75.6 [H36]
            systemic lipidoses E75.6 [H36]
        involving
            pigment epithelium H35.54
            sensory area H35.53
        pigmentary H35.52
        vitreoretinal H35.51
    Salzmann's nodular --see Degeneration, cornea, nodular
    scapuloperoneal G71.09
    skin NEC L98.8
    sympathetic (reflex) --see Syndrome, pain, complex regional I
        cervical G90.2
    tapetoretinal H35.54
    thoracic, asphyxiating Q77.2
    unguium L60.3
        congenital Q84.6
    vitreoretinal H35.51
    vulva N90.4
    yellow (liver) --see Failure, hepatic