ICD-10-CM Alphabetic Index to Diseases and Injuries
Dystrophy, dystrophia
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- 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 G71.039 — see also Dystrophy, muscular, limb-girdle, by type
- meaning Limb girdle muscular dystrophy NOS G71.039
- meaning Limb girdle muscular dystrophy, other specified type, — see by type
- meaning Limb girdle muscular dystrophy, specified type NEC G71.038
- meaning Limb girdle muscular dystrophy type 2A (autosomal recessive) G71.032
- 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 — see also Dystrophy, muscular, by type
- Landouzy-Déjérine type G71.02
- limb-girdle G71.039
- alpha-sarcoglycan-related G71.0341
- anoctamin-5-related autosomal recessive (R12) G71.035
- autosomal recessive NEC G71.038
- beta-sarcoglycan-related G71.0342
- calpain-3-related G71.032
- autosomal dominant G71.031
- autosomal recessive G71.032
- collagen VI related
- autosomal dominant G71.031
- autosomal recessive G71.038
- D1 (autosomal dominant) G71.031
- D2 (autosomal dominant) G71.031
- D3 (autosomal dominant) G71.031
- D4 (autosomal dominant) G71.031
- D5 (autosomal dominant) G71.031
- delta-sarcoglycan-related G71.0349
- due to
- alpha sarcoglycan dysfunction G71.0341
- anoctamin-5 dysfunction G71.035
- beta sarcoglycan dysfunction G71.0342
- fukutin related protein dysfunction G71.036
- sarcoglycan dysfunction, specified NEC G71.0349
- FKRP-related autosomal recessive G71.038
- gamma-sarcoglycan-related G71.0349
- R1 (autosomal recessive) G71.032
- R2 (autosomal recessive) G71.033
- R3 (autosomal recessive) G71.0341
- R4 (autosomal recessive) G71.0342
- R5 (autosomal recessive) G71.0349
- R6 (autosomal recessive) G71.0349
- R7 (autosomal recessive) G71.038
- R8 (autosomal recessive) G71.038
- R9 (autosomal recessive) G71.036
- R10 (autosomal recessive) G71.038
- R11 (autosomal recessive) G71.038
- R12 (autosomal recessive) G71.035
- R13 (autosomal recessive) G71.038
- R14 (autosomal recessive) G71.038
- R15 (autosomal recessive) G71.038
- R16 (autosomal recessive) G71.038
- R17 (autosomal recessive) G71.038
- R18 (autosomal recessive) G71.038
- R19 (autosomal recessive) G71.038
- R20 (autosomal recessive) G71.038
- R21 (autosomal recessive) G71.038
- R22 (autosomal recessive) G71.038
- R23 (autosomal recessive) G71.038
- R24 (autosomal recessive) G71.038
- type 1 (autosomal dominant) G71.031
- type 1A (autosomal dominant) G71.031
- type 1B (autosomal dominant) G71.031
- type 1C (autosomal dominant) G71.031
- type 1E (autosomal dominant) G71.031
- type 1H (autosomal dominant) G71.031
- type 1I (autosomal dominant) G71.031
- type 2 (autosomal recessive) G71.038
- specified NEC G71.038
- type 2A (autosomal recessive) G71.032
- type 2B (autosomal recessive) G71.033
- type 2C (autosomal recessive) G71.0349
- type 2D (autosomal recessive) G71.0341
- type 2E (autosomal recessive) G71.0342
- type 2F (autosomal recessive) G71.0349
- type 2G (autosomal recessive) G71.038
- type 2H (autosomal recessive) G71.038
- type 2I (autosomal recessive) G71.036
- type 2J (autosomal recessive) G71.038
- type 2K (autosomal recessive) G71.038
- type 2L (autosomal recessive) G71.035
- type 2M (autosomal recessive) G71.038
- type 2N (autosomal recessive) G71.038
- type 2O (autosomal recessive) G71.038
- type 2P (autosomal recessive) G71.038
- type 2Q (autosomal recessive) G71.038
- type 2S (autosomal recessive) G71.038
- type 2T (autosomal recessive) G71.038
- type 2U (autosomal recessive) G71.038
- myotonic G71.11
- progressive (hereditary) G71.09 — see also Dystrophy, muscular, by type
- Charcot-Marie (-Tooth) type 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
- systemic lipidoses E75.6
- 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