Dystrophy, dystrophia - in the ICD-10-CM Index

Annotation Back-References in the 2025 ICD-10-CM Index to Diseases and Injuries

Browse the ICD-10-CM codes with references applicable to the clinical term "dystrophy, dystrophia"

Dystrophy, dystrophia
- adiposogenital - E23.6 Other disorders of pituitary gland
- autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker - G71.01 Duchenne or Becker muscular dystrophy
- Becker's type - G71.01 Duchenne or Becker muscular dystrophy
- cervical sympathetic - G90.2 Horner's syndrome
- choroid (hereditary) - H31.20 Hereditary choroidal dystrophy, unspecified
  - central areolar - H31.22 Choroidal dystrophy (central areolar) (generalized) (peripapillary)
  - choroideremia - H31.21 Choroideremia
  - gyrate atrophy - H31.23 Gyrate atrophy, choroid
  - specified type NEC - H31.29 Other hereditary choroidal dystrophy
- cornea (hereditary) - H18.50 Unspecified hereditary corneal dystrophies
  - endothelial - H18.51 Endothelial corneal dystrophy
  - epithelial - H18.52 Epithelial (juvenile) corneal dystrophy
  - granular - H18.53 Granular corneal dystrophy
  - lattice - H18.54 Lattice corneal dystrophy
  - macular - H18.55 Macular corneal dystrophy
  - specified type NEC - H18.59 Other hereditary corneal dystrophies
- Duchenne's type - G71.01 Duchenne or Becker muscular dystrophy
- due to malnutrition - E45 Retarded development following protein-calorie malnutrition
- Erb's - G71.02 Facioscapulohumeral muscular dystrophy
- Fuchs' - H18.51 Endothelial corneal dystrophy
- Gower's muscular - G71.01 Duchenne or Becker muscular dystrophy
- hair - L67.8 Other hair color and hair shaft abnormalities
- infantile neuraxonal - G31.89 Other specified degenerative diseases of nervous system
- Landouzy-Déjérine - G71.02 Facioscapulohumeral muscular dystrophy
- Leyden-Möbius - See Also: Dystrophy, muscular, limb-girdle, by type; - G71.039 Limb girdle muscular dystrophy, unspecified
  - meaning Limb girdle muscular dystrophy NOS - G71.039 Limb girdle muscular dystrophy, unspecified
  - meaning Limb girdle muscular dystrophy type 2A (autosomal recessive) - G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
  - meaning Limb girdle muscular dystrophy, other specified type, - See: by type;
  - meaning Limb girdle muscular dystrophy, specified type NEC - G71.038 Other limb girdle muscular dystrophy
- muscular - G71.00 Muscular dystrophy, unspecified
  - autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker - G71.01 Duchenne or Becker muscular dystrophy
  - benign (Becker type) - G71.01 Duchenne or Becker muscular dystrophy
    - scapuloperoneal with early contractures [Emery-Dreifuss] - G71.09 Other specified muscular dystrophies
  - congenital (hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber) - G71.09 Other specified muscular dystrophies
    - myotonic - G71.11 Myotonic muscular dystrophy
  - distal - G71.09 Other specified muscular dystrophies
  - Duchenne type - G71.01 Duchenne or Becker muscular dystrophy
  - Emery-Dreifuss - G71.09 Other specified muscular dystrophies
  - Erb type - G71.02 Facioscapulohumeral muscular dystrophy
  - facioscapulohumeral - G71.02 Facioscapulohumeral muscular dystrophy
  - Gower's - G71.01 Duchenne or Becker muscular dystrophy
  - hereditary (progressive) - See Also: Dystrophy, muscular, by type; - G71.09 Other specified muscular dystrophies
  - Landouzy-Déjérine type - G71.02 Facioscapulohumeral muscular dystrophy
  - limb-girdle - G71.039 Limb girdle muscular dystrophy, unspecified
    - alpha-sarcoglycan-related - G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
    - anoctamin-5-related autosomal recessive (R12) - G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
    - autosomal recessive NEC - G71.038 Other limb girdle muscular dystrophy
    - beta-sarcoglycan-related - G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
    - calpain-3-related - G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
      - autosomal dominant - G71.031 Autosomal dominant limb girdle muscular dystrophy
      - autosomal recessive - G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
    - collagen VI related
      - autosomal dominant - G71.031 Autosomal dominant limb girdle muscular dystrophy
      - autosomal recessive - G71.038 Other limb girdle muscular dystrophy
    - D1 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - D2 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - D3 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - D4 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - D5 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - delta-sarcoglycan-related - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
    - due to
      - alpha sarcoglycan dysfunction - G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
      - anoctamin-5 dysfunction - G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
      - beta sarcoglycan dysfunction - G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
      - fukutin related protein dysfunction - G71.038 Other limb girdle muscular dystrophy
      - sarcoglycan dysfunction, specified NEC - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
    - FKRP-related autosomal recessive - G71.038 Other limb girdle muscular dystrophy
    - gamma-sarcoglycan-related - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
    - R1 (autosomal recessive) - G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
    - R10 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R11 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R12 (autosomal recessive) - G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
    - R13 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R14 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R15 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R16 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R17 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R18 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R19 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R2 (autosomal recessive) - G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction
    - R20 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R21 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R22 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R23 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R24 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R3 (autosomal recessive) - G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
    - R4 (autosomal recessive) - G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
    - R5 (autosomal recessive) - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
    - R6 (autosomal recessive) - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
    - R7 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R8 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - R9 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - type 1 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - type 1A (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - type 1B (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - type 1C (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - type 1E (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - type 1H (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - type 1I (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
    - type 2 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
      - specified NEC - G71.038 Other limb girdle muscular dystrophy
    - type 2A (autosomal recessive) - G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
    - type 2B (autosomal recessive) - G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction
    - type 2C (autosomal recessive) - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
    - type 2D (autosomal recessive) - G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
    - type 2E (autosomal recessive) - G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
    - type 2F (autosomal recessive) - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
    - type 2I (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
    - type 2L (autosomal recessive) - G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
  - myotonic - G71.11 Myotonic muscular dystrophy
  - progressive (hereditary) - See Also: Dystrophy, muscular, by type; - G71.09 Other specified muscular dystrophies
    - Charcot-Marie (-Tooth) type - G60.0 Hereditary motor and sensory neuropathy
  - pseudohypertrophic (infantile) - G71.01 Duchenne or Becker muscular dystrophy
  - scapulohumeral - G71.02 Facioscapulohumeral muscular dystrophy
  - scapuloperoneal - G71.09 Other specified muscular dystrophies
  - severe (Duchenne type) - G71.01 Duchenne or Becker muscular dystrophy
  - specified type NEC - G71.09 Other specified muscular dystrophies
- myocardium, myocardial - See: Degeneration, myocardial;
- myotonic, myotonica - G71.11 Myotonic muscular dystrophy
- nail - L60.3 Nail dystrophy
  - congenital - Q84.6 Other congenital malformations of nails
- nutritional - E45 Retarded development following protein-calorie malnutrition
- ocular - G71.09 Other specified muscular dystrophies
- oculocerebrorenal - E72.03 Lowe's syndrome
- oculopharyngeal - G71.09 Other specified muscular dystrophies
- ovarian - N83.8 Other noninflammatory disorders of ovary, fallopian tube and broad ligament
- polyglandular - E31.8 Other polyglandular dysfunction
- reflex (neuromuscular) (sympathetic) - See: Syndrome, pain, complex regional I;
- retinal (hereditary) - H35.50 Unspecified hereditary retinal dystrophy
  - in
    - lipid storage disorders - E75.6 Lipid storage disorder, unspecified
    - systemic lipidoses - E75.6 Lipid storage disorder, unspecified
  - involving
    - pigment epithelium - H35.54 Dystrophies primarily involving the retinal pigment epithelium
    - sensory area - H35.53 Other dystrophies primarily involving the sensory retina
  - pigmentary - H35.52 Pigmentary retinal dystrophy
  - vitreoretinal - H35.51 Vitreoretinal dystrophy
- Salzmann's nodular - See: Degeneration, cornea, nodular;
- scapuloperoneal - G71.09 Other specified muscular dystrophies
- skin NEC - L98.8 Other specified disorders of the skin and subcutaneous tissue
- sympathetic (reflex) - See: Syndrome, pain, complex regional I;
  - cervical - G90.2 Horner's syndrome
- tapetoretinal - H35.54 Dystrophies primarily involving the retinal pigment epithelium
- thoracic, asphyxiating - Q77.2 Short rib syndrome
- unguium - L60.3 Nail dystrophy
  - congenital - Q84.6 Other congenital malformations of nails
- vitreoretinal - H35.51 Vitreoretinal dystrophy
- vulva - N90.4 Leukoplakia of vulva
- yellow (liver) - See: Failure, hepatic;

Applicable Clinical Terms Definitions

Hair: A filament-like structure consisting of a shaft which projects to the surface of the SKIN from a root which is softer than the shaft and lodges in the cavity of a HAIR FOLLICLE. It is found on most surfaces of the body.

Nails: The thin, horny plates that cover the dorsal surfaces of the distal phalanges of the fingers and toes of primates.

Vulva: The external genitalia of the female. It includes the CLITORIS, the labia, the vestibule, and its glands.

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