1. 2023 ICD-10-CM Index
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2. 'D' Terms
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3. Index Terms Starting With 'D' (Dystrophy, dystrophia)

Index Terms Starting With 'D' (Dystrophy, dystrophia)

• Dystrophy, dystrophia

  • adiposogenital E23.6
    ICD-10-CM Diagnosis Code E23.6

    Other disorders of pituitary gland

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Abscess of pituitary
    • Adiposogenital dystrophy
  • autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker G71.01
    ICD-10-CM Diagnosis Code G71.01

    Duchenne or Becker muscular dystrophy

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
    • Benign [Becker] muscular dystrophy
    • Severe [Duchenne] muscular dystrophy
  • Becker's type G71.01
    ICD-10-CM Diagnosis Code G71.01

    Duchenne or Becker muscular dystrophy

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
    • Benign [Becker] muscular dystrophy
    • Severe [Duchenne] muscular dystrophy
  • cervical sympathetic G90.2
    ICD-10-CM Diagnosis Code G90.2

    Horner's syndrome

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Bernard(-Horner) syndrome
    • Cervical sympathetic dystrophy or paralysis
  • choroid (hereditary) H31.20
    ICD-10-CM Diagnosis Code H31.20

    Hereditary choroidal dystrophy, unspecified

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    • central areolar H31.22
      ICD-10-CM Diagnosis Code H31.22

      Choroidal dystrophy (central areolar) (generalized) (peripapillary)

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    • choroideremia H31.21
      ICD-10-CM Diagnosis Code H31.21

      Choroideremia

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    • gyrate atrophy H31.23
      ICD-10-CM Diagnosis Code H31.23

      Gyrate atrophy, choroid

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    • specified type NEC H31.29
      ICD-10-CM Diagnosis Code H31.29

      Other hereditary choroidal dystrophy

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
  • cornea (hereditary) H18.50-
    ICD-10-CM Diagnosis Code H18.50-

    Unspecified hereditary corneal dystrophies

    2016 2017 2018 2019 2020 2021 - Converted to Parent Code 2022 2023 Non-Billable/Non-Specific Code
    • endothelial H18.51-
      ICD-10-CM Diagnosis Code H18.51-

      Endothelial corneal dystrophy

      2016 2017 2018 2019 2020 2021 - Converted to Parent Code 2022 2023 Non-Billable/Non-Specific Code

      Applicable To

      • Fuchs' dystrophy
    • epithelial H18.52-
      ICD-10-CM Diagnosis Code H18.52-

      Epithelial (juvenile) corneal dystrophy

      2016 2017 2018 2019 2020 2021 - Converted to Parent Code 2022 2023 Non-Billable/Non-Specific Code
    • granular H18.53-
      ICD-10-CM Diagnosis Code H18.53-

      Granular corneal dystrophy

      2016 2017 2018 2019 2020 2021 - Converted to Parent Code 2022 2023 Non-Billable/Non-Specific Code
    • lattice H18.54-
      ICD-10-CM Diagnosis Code H18.54-

      Lattice corneal dystrophy

      2016 2017 2018 2019 2020 2021 - Converted to Parent Code 2022 2023 Non-Billable/Non-Specific Code
    • macular H18.55-
      ICD-10-CM Diagnosis Code H18.55-

      Macular corneal dystrophy

      2016 2017 2018 2019 2020 2021 - Converted to Parent Code 2022 2023 Non-Billable/Non-Specific Code
    • specified type NEC H18.59-
      ICD-10-CM Diagnosis Code H18.59-

      Other hereditary corneal dystrophies

      2016 2017 2018 2019 2020 2021 - Converted to Parent Code 2022 2023 Non-Billable/Non-Specific Code
  • Duchenne's type G71.01
    ICD-10-CM Diagnosis Code G71.01

    Duchenne or Becker muscular dystrophy

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
    • Benign [Becker] muscular dystrophy
    • Severe [Duchenne] muscular dystrophy
  • due to malnutrition E45
    ICD-10-CM Diagnosis Code E45

    Retarded development following protein-calorie malnutrition

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Nutritional short stature
    • Nutritional stunting
    • Physical retardation due to malnutrition
  • Erb's G71.02
    ICD-10-CM Diagnosis Code G71.02

    Facioscapulohumeral muscular dystrophy

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Scapulohumeral muscular dystrophy
  • Fuchs' H18.51-
    ICD-10-CM Diagnosis Code H18.51-

    Endothelial corneal dystrophy

    2016 2017 2018 2019 2020 2021 - Converted to Parent Code 2022 2023 Non-Billable/Non-Specific Code

    Applicable To

    • Fuchs' dystrophy
  • Gower's muscular G71.01
    ICD-10-CM Diagnosis Code G71.01

    Duchenne or Becker muscular dystrophy

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
    • Benign [Becker] muscular dystrophy
    • Severe [Duchenne] muscular dystrophy
  • hair L67.8
    ICD-10-CM Diagnosis Code L67.8

    Other hair color and hair shaft abnormalities

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Fragilitas crinium
  • infantile neuraxonal G31.89
    ICD-10-CM Diagnosis Code G31.89

    Other specified degenerative diseases of nervous system

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
  • Landouzy-Déjérine G71.02
    ICD-10-CM Diagnosis Code G71.02

    Facioscapulohumeral muscular dystrophy

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Scapulohumeral muscular dystrophy
  • Leyden-Möbius G71.039
    - see also Dystrophy, muscular, limb-girdle, by type
    ICD-10-CM Diagnosis Code G71.039

    Limb girdle muscular dystrophy, unspecified

    2023 - New Code Billable/Specific Code
    • meaning Limb girdle muscular dystrophy NOS G71.039
      ICD-10-CM Diagnosis Code G71.039

      Limb girdle muscular dystrophy, unspecified

      2023 - New Code Billable/Specific Code
    • meaning Limb girdle muscular dystrophy type 2A G71.032
      (autosomal recessive)
      ICD-10-CM Diagnosis Code G71.032

      Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

      2023 - New Code Billable/Specific Code

      Applicable To

      • Limb girdle muscular dystrophy type 2A
      • LGMD R1 calpain-3-related
      • Primary calpainopathy
    • meaning Limb girdle muscular dystrophy, other specified type, - see by type
    • meaning Limb girdle muscular dystrophy, specified type NEC G71.038
      ICD-10-CM Diagnosis Code G71.038

      Other limb girdle muscular dystrophy

      2023 - New Code Billable/Specific Code

      Applicable To

      • LGMD R9 FKRP-related
      • LGMD R22 collagen 6-related
      • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
      • Limb girdle muscular dystrophy type 2I
      • Other autosomal recessive limb girdle muscular dystrophy
  • muscular G71.00
    ICD-10-CM Diagnosis Code G71.00

    Muscular dystrophy, unspecified

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code
    • autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker G71.01
      ICD-10-CM Diagnosis Code G71.01

      Duchenne or Becker muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
      • Benign [Becker] muscular dystrophy
      • Severe [Duchenne] muscular dystrophy
    • benign (Becker type) G71.01
      ICD-10-CM Diagnosis Code G71.01

      Duchenne or Becker muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
      • Benign [Becker] muscular dystrophy
      • Severe [Duchenne] muscular dystrophy
      • scapuloperoneal with early contractures [Emery-Dreifuss] G71.09
        ICD-10-CM Diagnosis Code G71.09

        Other specified muscular dystrophies

        2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

        Applicable To

        • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
        • Congenital muscular dystrophy NOS
        • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
        • Distal muscular dystrophy
        • Ocular muscular dystrophy
        • Oculopharyngeal muscular dystrophy
        • Scapuloperoneal muscular dystrophy
    • congenital (hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber) G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
      • myotonic G71.11
        ICD-10-CM Diagnosis Code G71.11

        Myotonic muscular dystrophy

        2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

        Applicable To

        • Dystrophia myotonica [Steinert]
        • Myotonia atrophica
        • Myotonic dystrophy
        • Proximal myotonic myopathy (PROMM)
        • Steinert disease
    • distal G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
    • Duchenne type G71.01
      ICD-10-CM Diagnosis Code G71.01

      Duchenne or Becker muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
      • Benign [Becker] muscular dystrophy
      • Severe [Duchenne] muscular dystrophy
    • Emery-Dreifuss G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
    • Erb type G71.02
      ICD-10-CM Diagnosis Code G71.02

      Facioscapulohumeral muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Scapulohumeral muscular dystrophy
    • facioscapulohumeral G71.02
      ICD-10-CM Diagnosis Code G71.02

      Facioscapulohumeral muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Scapulohumeral muscular dystrophy
    • Gower's G71.01
      ICD-10-CM Diagnosis Code G71.01

      Duchenne or Becker muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
      • Benign [Becker] muscular dystrophy
      • Severe [Duchenne] muscular dystrophy
    • hereditary G71.09
      (progressive) - see also Dystrophy, muscular, by type
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
    • Landouzy-Déjérine type G71.02
      ICD-10-CM Diagnosis Code G71.02

      Facioscapulohumeral muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Scapulohumeral muscular dystrophy
    • limb-girdle G71.039
      ICD-10-CM Diagnosis Code G71.039

      Limb girdle muscular dystrophy, unspecified

      2023 - New Code Billable/Specific Code
      • alpha-sarcoglycan-related G71.0341
        ICD-10-CM Diagnosis Code G71.0341

        Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Alpha sarcoglycanopathy
        • Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
        • Limb girdle muscular dystrophy type 2D
      • anoctamin-5-related autosomal recessive G71.035
        (R12)
        ICD-10-CM Diagnosis Code G71.035

        Limb girdle muscular dystrophy due to anoctamin-5 dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Anoctamin-5-related LGMD R12
        • Anoctaminopathy
        • Autosomal recessive limb girdle muscular dystrophy type 2L
        • Miyoshi myopathy type 3
      • autosomal recessive NEC G71.038
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • beta-sarcoglycan-related G71.0342
        ICD-10-CM Diagnosis Code G71.0342

        Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Beta sarcoglycanopathy
        • Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency
        • Limb girdle muscular dystrophy type 2E
      • calpain-3-related G71.032
        ICD-10-CM Diagnosis Code G71.032

        Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Limb girdle muscular dystrophy type 2A
        • LGMD R1 calpain-3-related
        • Primary calpainopathy
        • autosomal dominant G71.031
          ICD-10-CM Diagnosis Code G71.031

          Autosomal dominant limb girdle muscular dystrophy

          2023 - New Code Billable/Specific Code

          Applicable To

          • LGMD D4 calpain-3-related
          • LGMD D5 collagen 6-related
          • Limb girdle muscular dystrophy type 1
        • autosomal recessive G71.032
          ICD-10-CM Diagnosis Code G71.032

          Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

          2023 - New Code Billable/Specific Code

          Applicable To

          • Limb girdle muscular dystrophy type 2A
          • LGMD R1 calpain-3-related
          • Primary calpainopathy
      • collagen VI related
        • autosomal dominant G71.031
          ICD-10-CM Diagnosis Code G71.031

          Autosomal dominant limb girdle muscular dystrophy

          2023 - New Code Billable/Specific Code

          Applicable To

          • LGMD D4 calpain-3-related
          • LGMD D5 collagen 6-related
          • Limb girdle muscular dystrophy type 1
        • autosomal recessive G71.038
          ICD-10-CM Diagnosis Code G71.038

          Other limb girdle muscular dystrophy

          2023 - New Code Billable/Specific Code

          Applicable To

          • LGMD R9 FKRP-related
          • LGMD R22 collagen 6-related
          • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
          • Limb girdle muscular dystrophy type 2I
          • Other autosomal recessive limb girdle muscular dystrophy
      • D1 G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • D2 G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • D3 G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • D4 G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • D5 G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • delta-sarcoglycan-related G71.0349
        ICD-10-CM Diagnosis Code G71.0349

        Limb girdle muscular dystrophy due to other sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Delta sarcoglycanopathy
        • Delta-sarcoglycan-related LGMD R6
        • Gamma sarcoglycanopathy
        • Gamma-sarcoglycan-related LGMD R5
        • Limb girdle muscular dystrophy type 2C
        • Limb girdle muscular dystrophy type 2F
      • due to
        • alpha sarcoglycan dysfunction G71.0341
          ICD-10-CM Diagnosis Code G71.0341

          Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction

          2023 - New Code Billable/Specific Code

          Applicable To

          • Alpha sarcoglycanopathy
          • Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
          • Limb girdle muscular dystrophy type 2D
        • anoctamin-5 dysfunction G71.035
          ICD-10-CM Diagnosis Code G71.035

          Limb girdle muscular dystrophy due to anoctamin-5 dysfunction

          2023 - New Code Billable/Specific Code

          Applicable To

          • Anoctamin-5-related LGMD R12
          • Anoctaminopathy
          • Autosomal recessive limb girdle muscular dystrophy type 2L
          • Miyoshi myopathy type 3
        • beta sarcoglycan dysfunction G71.0342
          ICD-10-CM Diagnosis Code G71.0342

          Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction

          2023 - New Code Billable/Specific Code

          Applicable To

          • Beta sarcoglycanopathy
          • Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency
          • Limb girdle muscular dystrophy type 2E
        • fukutin related protein dysfunction G71.038
          ICD-10-CM Diagnosis Code G71.038

          Other limb girdle muscular dystrophy

          2023 - New Code Billable/Specific Code

          Applicable To

          • LGMD R9 FKRP-related
          • LGMD R22 collagen 6-related
          • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
          • Limb girdle muscular dystrophy type 2I
          • Other autosomal recessive limb girdle muscular dystrophy
        • sarcoglycan dysfunction, specified NEC G71.0349
          ICD-10-CM Diagnosis Code G71.0349

          Limb girdle muscular dystrophy due to other sarcoglycan dysfunction

          2023 - New Code Billable/Specific Code

          Applicable To

          • Delta sarcoglycanopathy
          • Delta-sarcoglycan-related LGMD R6
          • Gamma sarcoglycanopathy
          • Gamma-sarcoglycan-related LGMD R5
          • Limb girdle muscular dystrophy type 2C
          • Limb girdle muscular dystrophy type 2F
      • FKRP-related autosomal recessive G71.038
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • gamma-sarcoglycan-related G71.0349
        ICD-10-CM Diagnosis Code G71.0349

        Limb girdle muscular dystrophy due to other sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Delta sarcoglycanopathy
        • Delta-sarcoglycan-related LGMD R6
        • Gamma sarcoglycanopathy
        • Gamma-sarcoglycan-related LGMD R5
        • Limb girdle muscular dystrophy type 2C
        • Limb girdle muscular dystrophy type 2F
      • R1 G71.032
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.032

        Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Limb girdle muscular dystrophy type 2A
        • LGMD R1 calpain-3-related
        • Primary calpainopathy
      • R10 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R11 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R12 G71.035
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.035

        Limb girdle muscular dystrophy due to anoctamin-5 dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Anoctamin-5-related LGMD R12
        • Anoctaminopathy
        • Autosomal recessive limb girdle muscular dystrophy type 2L
        • Miyoshi myopathy type 3
      • R13 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R14 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R15 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R16 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R17 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R18 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R19 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R2 G71.033
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.033

        Limb girdle muscular dystrophy due to dysferlin dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Dysferlinopathy
        • LGMD R2 dysferlin-related
        • Limb girdle muscular dystrophy type 2B
        • Miyoshi Myopathy type 1
      • R20 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R21 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R22 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R23 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R24 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R3 G71.0341
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.0341

        Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Alpha sarcoglycanopathy
        • Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
        • Limb girdle muscular dystrophy type 2D
      • R4 G71.0342
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.0342

        Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Beta sarcoglycanopathy
        • Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency
        • Limb girdle muscular dystrophy type 2E
      • R5 G71.0349
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.0349

        Limb girdle muscular dystrophy due to other sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Delta sarcoglycanopathy
        • Delta-sarcoglycan-related LGMD R6
        • Gamma sarcoglycanopathy
        • Gamma-sarcoglycan-related LGMD R5
        • Limb girdle muscular dystrophy type 2C
        • Limb girdle muscular dystrophy type 2F
      • R6 G71.0349
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.0349

        Limb girdle muscular dystrophy due to other sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Delta sarcoglycanopathy
        • Delta-sarcoglycan-related LGMD R6
        • Gamma sarcoglycanopathy
        • Gamma-sarcoglycan-related LGMD R5
        • Limb girdle muscular dystrophy type 2C
        • Limb girdle muscular dystrophy type 2F
      • R7 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R8 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • R9 G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • type 1 G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • type 1A G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • type 1B G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • type 1C G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • type 1E G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • type 1H G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • type 1I G71.031
        (autosomal dominant)
        ICD-10-CM Diagnosis Code G71.031

        Autosomal dominant limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD D4 calpain-3-related
        • LGMD D5 collagen 6-related
        • Limb girdle muscular dystrophy type 1
      • type 2 (autosomal recessive) G71.038
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
        • specified NEC G71.038
          ICD-10-CM Diagnosis Code G71.038

          Other limb girdle muscular dystrophy

          2023 - New Code Billable/Specific Code

          Applicable To

          • LGMD R9 FKRP-related
          • LGMD R22 collagen 6-related
          • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
          • Limb girdle muscular dystrophy type 2I
          • Other autosomal recessive limb girdle muscular dystrophy
      • type 2A G71.032
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.032

        Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Limb girdle muscular dystrophy type 2A
        • LGMD R1 calpain-3-related
        • Primary calpainopathy
      • type 2B G71.033
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.033

        Limb girdle muscular dystrophy due to dysferlin dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Dysferlinopathy
        • LGMD R2 dysferlin-related
        • Limb girdle muscular dystrophy type 2B
        • Miyoshi Myopathy type 1
      • type 2C G71.0349
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.0349

        Limb girdle muscular dystrophy due to other sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Delta sarcoglycanopathy
        • Delta-sarcoglycan-related LGMD R6
        • Gamma sarcoglycanopathy
        • Gamma-sarcoglycan-related LGMD R5
        • Limb girdle muscular dystrophy type 2C
        • Limb girdle muscular dystrophy type 2F
      • type 2D G71.0341
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.0341

        Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Alpha sarcoglycanopathy
        • Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
        • Limb girdle muscular dystrophy type 2D
      • type 2E G71.0342
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.0342

        Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Beta sarcoglycanopathy
        • Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency
        • Limb girdle muscular dystrophy type 2E
      • type 2F G71.0349
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.0349

        Limb girdle muscular dystrophy due to other sarcoglycan dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Delta sarcoglycanopathy
        • Delta-sarcoglycan-related LGMD R6
        • Gamma sarcoglycanopathy
        • Gamma-sarcoglycan-related LGMD R5
        • Limb girdle muscular dystrophy type 2C
        • Limb girdle muscular dystrophy type 2F
      • type 2I G71.038
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.038

        Other limb girdle muscular dystrophy

        2023 - New Code Billable/Specific Code

        Applicable To

        • LGMD R9 FKRP-related
        • LGMD R22 collagen 6-related
        • Limb girdle muscular dystrophy due to fukutin related protein dysfunction
        • Limb girdle muscular dystrophy type 2I
        • Other autosomal recessive limb girdle muscular dystrophy
      • type 2L G71.035
        (autosomal recessive)
        ICD-10-CM Diagnosis Code G71.035

        Limb girdle muscular dystrophy due to anoctamin-5 dysfunction

        2023 - New Code Billable/Specific Code

        Applicable To

        • Anoctamin-5-related LGMD R12
        • Anoctaminopathy
        • Autosomal recessive limb girdle muscular dystrophy type 2L
        • Miyoshi myopathy type 3
    • myotonic G71.11
      ICD-10-CM Diagnosis Code G71.11

      Myotonic muscular dystrophy

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Dystrophia myotonica [Steinert]
      • Myotonia atrophica
      • Myotonic dystrophy
      • Proximal myotonic myopathy (PROMM)
      • Steinert disease
    • progressive (hereditary) G71.09
      - see also Dystrophy, muscular, by type
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
      • Charcot-Marie G60.0
        (-Tooth)
        ICD-10-CM Diagnosis Code G60.0

        Hereditary motor and sensory neuropathy

        2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

        Applicable To

        • Charcot-Marie-Tooth disease
        • Déjérine-Sottas disease
        • Hereditary motor and sensory neuropathy, types I-IV
        • Hypertrophic neuropathy of infancy
        • Peroneal muscular atrophy (axonal type) (hypertrophic type)
        • Roussy-Levy syndrome
    • pseudohypertrophic G71.01
      (infantile)
      ICD-10-CM Diagnosis Code G71.01

      Duchenne or Becker muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
      • Benign [Becker] muscular dystrophy
      • Severe [Duchenne] muscular dystrophy
    • scapulohumeral G71.02
      ICD-10-CM Diagnosis Code G71.02

      Facioscapulohumeral muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Scapulohumeral muscular dystrophy
    • scapuloperoneal G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
    • severe G71.01
      (Duchenne type)
      ICD-10-CM Diagnosis Code G71.01

      Duchenne or Becker muscular dystrophy

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker muscular dystrophy
      • Benign [Becker] muscular dystrophy
      • Severe [Duchenne] muscular dystrophy
    • specified type NEC G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

      2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
      • Congenital muscular dystrophy NOS
      • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
      • Distal muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
  • myocardium, myocardial - see Degeneration, myocardial
  • myotonic, myotonica G71.11
    ICD-10-CM Diagnosis Code G71.11

    Myotonic muscular dystrophy

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Dystrophia myotonica [Steinert]
    • Myotonia atrophica
    • Myotonic dystrophy
    • Proximal myotonic myopathy (PROMM)
    • Steinert disease
  • nail L60.3
    ICD-10-CM Diagnosis Code L60.3

    Nail dystrophy

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    • congenital Q84.6
      ICD-10-CM Diagnosis Code Q84.6

      Other congenital malformations of nails

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt

      Applicable To

      • Congenital clubnail
      • Congenital koilonychia
      • Congenital malformation of nail NOS
  • nutritional E45
    ICD-10-CM Diagnosis Code E45

    Retarded development following protein-calorie malnutrition

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Nutritional short stature
    • Nutritional stunting
    • Physical retardation due to malnutrition
  • ocular G71.09
    ICD-10-CM Diagnosis Code G71.09

    Other specified muscular dystrophies

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
    • Congenital muscular dystrophy NOS
    • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
    • Distal muscular dystrophy
    • Ocular muscular dystrophy
    • Oculopharyngeal muscular dystrophy
    • Scapuloperoneal muscular dystrophy
  • oculocerebrorenal E72.03
    ICD-10-CM Diagnosis Code E72.03

    Lowe's syndrome

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Use Additional

    • code for associated glaucoma (H42)
  • oculopharyngeal G71.09
    ICD-10-CM Diagnosis Code G71.09

    Other specified muscular dystrophies

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
    • Congenital muscular dystrophy NOS
    • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
    • Distal muscular dystrophy
    • Ocular muscular dystrophy
    • Oculopharyngeal muscular dystrophy
    • Scapuloperoneal muscular dystrophy
  • ovarian N83.8
    ICD-10-CM Diagnosis Code N83.8

    Other noninflammatory disorders of ovary, fallopian tube and broad ligament

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code Female Dx

    Applicable To

    • Broad ligament laceration syndrome [Allen-Masters]
  • polyglandular E31.8
    ICD-10-CM Diagnosis Code E31.8

    Other polyglandular dysfunction

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
  • reflex (neuromuscular) (sympathetic) - see Syndrome, pain, complex regional I
  • retinal (hereditary) H35.50
    ICD-10-CM Diagnosis Code H35.50

    Unspecified hereditary retinal dystrophy

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    • in
      • lipid storage disorders E75.6
        ICD-10-CM Diagnosis Code E75.6

        Lipid storage disorder, unspecified

        2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
      • systemic lipidoses E75.6
        ICD-10-CM Diagnosis Code E75.6

        Lipid storage disorder, unspecified

        2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    • involving
      • pigment epithelium H35.54
        ICD-10-CM Diagnosis Code H35.54

        Dystrophies primarily involving the retinal pigment epithelium

        2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

        Applicable To

        • Vitelliform retinal dystrophy
      • sensory area H35.53
        ICD-10-CM Diagnosis Code H35.53

        Other dystrophies primarily involving the sensory retina

        2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

        Applicable To

        • Stargardt's disease
    • pigmentary H35.52
      ICD-10-CM Diagnosis Code H35.52

      Pigmentary retinal dystrophy

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Albipunctate retinal dystrophy
      • Retinitis pigmentosa
      • Tapetoretinal dystrophy
    • vitreoretinal H35.51
      ICD-10-CM Diagnosis Code H35.51

      Vitreoretinal dystrophy

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
  • Salzmann's nodular - see Degeneration, cornea, nodular
  • scapuloperoneal G71.09
    ICD-10-CM Diagnosis Code G71.09

    Other specified muscular dystrophies

    2019 - New Code 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
    • Congenital muscular dystrophy NOS
    • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
    • Distal muscular dystrophy
    • Ocular muscular dystrophy
    • Oculopharyngeal muscular dystrophy
    • Scapuloperoneal muscular dystrophy
  • skin NEC L98.8
    ICD-10-CM Diagnosis Code L98.8

    Other specified disorders of the skin and subcutaneous tissue

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
  • sympathetic (reflex) - see Syndrome, pain, complex regional I
    • cervical G90.2
      ICD-10-CM Diagnosis Code G90.2

      Horner's syndrome

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

      Applicable To

      • Bernard(-Horner) syndrome
      • Cervical sympathetic dystrophy or paralysis
  • tapetoretinal H35.54
    ICD-10-CM Diagnosis Code H35.54

    Dystrophies primarily involving the retinal pigment epithelium

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

    Applicable To

    • Vitelliform retinal dystrophy
  • thoracic, asphyxiating Q77.2
    ICD-10-CM Diagnosis Code Q77.2

    Short rib syndrome

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt

    Applicable To

    • Asphyxiating thoracic dysplasia [Jeune]
  • unguium L60.3
    ICD-10-CM Diagnosis Code L60.3

    Nail dystrophy

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
    • congenital Q84.6
      ICD-10-CM Diagnosis Code Q84.6

      Other congenital malformations of nails

      2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt

      Applicable To

      • Congenital clubnail
      • Congenital koilonychia
      • Congenital malformation of nail NOS
  • vitreoretinal H35.51
    ICD-10-CM Diagnosis Code H35.51

    Vitreoretinal dystrophy

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
  • vulva N90.4
    ICD-10-CM Diagnosis Code N90.4

    Leukoplakia of vulva

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code Female Dx

    Applicable To

    • Dystrophy of vulva
    • Kraurosis of vulva
    • Lichen sclerosus of external female genital organs
  • yellow (liver) - see Failure, hepatic