Alphabetic Index · main term

Dystrophy, dystrophia

FY2027Index: Dw–Dy /Alphabetic Index

Dystrophy, dystrophia is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). It has 161 subterms and 151 code entries. First-level subterms include adiposogenital, autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker, Becker's type, cervical sympathetic, choroid, cornea, Duchenne's type, due to malnutrition and more. Confirm any code you find here in the Tabular List before you report it.

Subterms 161

adiposogenitalE23.6
autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or BeckerG71.01
Becker's typeG71.01
cervical sympatheticG90.2
choroid (hereditary)H31.20
- central areolarH31.22
- choroideremiaH31.21
- gyrate atrophyH31.23
- specified type NECH31.29
cornea (hereditary)H18.50-
- endothelialH18.51-
- epithelialH18.52-
- granularH18.53-
- latticeH18.54-
- macularH18.55-
- specified type NECH18.59-
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
Leyden-Möbius see also Dystrophy, muscular, limb-girdle, by typeG71.039
- meaning Limb girdle muscular dystrophy NOSG71.039
- meaning Limb girdle muscular dystrophy, other specified type, see by type
- meaning Limb girdle muscular dystrophy, specified type NECG71.038
- meaning Limb girdle muscular dystrophy type 2A (autosomal recessive)G71.032
muscularG71.00
- autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or BeckerG71.01
- 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
  - myotonicG71.11
- distalG71.09
- Duchenne typeG71.01
- Emery-DreifussG71.09
- Erb typeG71.02
- facioscapulohumeralG71.02
- Gower'sG71.01
- hereditary (progressive) see also Dystrophy, muscular, by typeG71.09
- Landouzy-Déjérine typeG71.02
- limb-girdleG71.039
  - alpha-sarcoglycan-relatedG71.0341
  - anoctamin-5-related autosomal recessive (R12)G71.035
  - autosomal recessive NECG71.038
  - beta-sarcoglycan-relatedG71.0342
  - calpain-3-relatedG71.032
    autosomal dominantG71.031
    autosomal recessiveG71.032
  - collagen VI related
    autosomal dominantG71.031
    autosomal recessiveG71.038
  - 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-relatedG71.0349
  - due to
    alpha sarcoglycan dysfunctionG71.0341
    anoctamin-5 dysfunctionG71.035
    beta sarcoglycan dysfunctionG71.0342
    fukutin related protein dysfunctionG71.036
    sarcoglycan dysfunction, specified NECG71.0349
  - FKRP-related autosomal recessiveG71.038
  - gamma-sarcoglycan-relatedG71.0349
  - 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 NECG71.038
  - 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
- myotonicG71.11
- progressive (hereditary) see also Dystrophy, muscular, by typeG71.09
  - Charcot-Marie (-Tooth) typeG60.0
- pseudohypertrophic (infantile)G71.01
- scapulohumeralG71.02
- scapuloperonealG71.09
- severe (Duchenne type)G71.01
- specified type NECG71.09
myocardium, myocardial see Degeneration, myocardial
myotonic, myotonicaG71.11
nailL60.3
- congenitalQ84.6
nutritionalE45
ocularG71.09
oculocerebrorenalE72.03
oculopharyngealG71.09
ovarianN83.8
polyglandularE31.8
reflex (neuromuscular) (sympathetic) see Syndrome, pain, complex regional I
retinal (hereditary)H35.50
- in
  - lipid storage disordersE75.6[H36.89]
  - systemic lipidosesE75.6[H36.89]
- involving
  - pigment epitheliumH35.54
  - sensory areaH35.53
- pigmentaryH35.52
- vitreoretinalH35.51
Salzmann's nodular see Degeneration, cornea, nodular
scapuloperonealG71.09
skin NECL98.8
sympathetic (reflex) see Syndrome, pain, complex regional I
- cervicalG90.2
tapetoretinalH35.54
thoracic, asphyxiatingQ77.2
unguiumL60.3
- congenitalQ84.6
vitreoretinalH35.51
vulvaN90.4
yellow (liver) see Failure, hepatic