ICD-10-CM Alphabetic Index · FY 2027 162 Entries
Dystrophy in the ICD-10-CM Index ICD-10-CM
The main term Dystrophy, dystrophia carries 162 index entries pointing to 47 ICD-10-CM codes. Every indented line below refines the term by site, cause, or type. Verify any candidate code in the Tabular List before using it.
✓ Built from the official CMS FY 2027 index fileEffective Oct 1, 2026 – Sep 30, 2027
162
Index Entries
47
Codes Referenced
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Default Code
D
Letter
162 of 162 shown
ICD-10-CM
Index Entries Under Dystrophy 162 entries · 47 codes
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 Non-billable
endothelial H18.51 Non-billable
epithelial H18.52 Non-billable
granular H18.53 Non-billable
lattice H18.54 Non-billable
macular H18.55 Non-billable
specified type NEC H18.59 Non-billable
Duchenne's type G71.01
due to malnutrition E45
Erb's G71.02
Fuchs' H18.51 Non-billable
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
autosomal recessive NEC G71.038
autosomal dominant G71.031
autosomal recessive G71.032
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
due to
alpha sarcoglycan dysfunction G71.0341
anoctamin-5 dysfunction G71.035
beta sarcoglycan dysfunction G71.0342
sarcoglycan dysfunction, specified NEC 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
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
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Related Index Terms
Source: Centers for Medicare & Medicaid Services, FY 2027 ICD-10-CM Index to Diseases and Injuries release files, effective October 1, 2026 through September 30, 2027.
