ICD-10-CM Alphabetic Index
Dystrophy, dystrophia
Sub-terms(37)
—choroid(hereditary)H31.20—cornea(hereditary)H18.50—Leyden-MöbiusG71.039—muscularG71.00—nailL60.3—retinal(hereditary)H35.50—sympathetic(reflex)see Syndrome, pain, complex regional I—unguiumL60.3—adiposogenitalE23.6—autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or BeckerG71.01—Becker's typeG71.01—cervical sympatheticG90.2—Duchenne's typeG71.01—due to malnutritionE45—Erb'sG71.02—Fuchs'H18.51—Gower's muscularG71.01—hairL67.8—infantile neuraxonalG31.89—Landouzy-DéjérineG71.02—myotonic, myotonicaG71.11—nutritionalE45—ocularG71.09—oculocerebrorenalE72.03—oculopharyngealG71.09—ovarianN83.8—polyglandularE31.8—scapuloperonealG71.09—skin NECL98.8—tapetoretinalH35.54—thoracic, asphyxiatingQ77.2—vitreoretinalH35.51—vulvaN90.4—myocardium, myocardialsee Degeneration, myocardial—reflex(neuromuscular) (sympathetic)see Syndrome, pain, complex regional I—Salzmann's nodularsee Degeneration, cornea, nodular—yellow(liver)see Failure, hepatic