• Dystrophy, dystrophia

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

      Other disorders of pituitary gland

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

        Choroideremia

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

        Gyrate atrophy, choroid

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

        Other hereditary choroidal dystrophy

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

      Unspecified hereditary corneal dystrophies

        2016 2017 2018 2019 2020 Billable/Specific Code
      • endothelial H18.51
        ICD-10-CM Diagnosis Code H18.51

        Endothelial corneal dystrophy

          2016 2017 2018 2019 2020 Billable/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 Billable/Specific Code
      • granular H18.53
        ICD-10-CM Diagnosis Code H18.53

        Granular corneal dystrophy

          2016 2017 2018 2019 2020 Billable/Specific Code
      • lattice H18.54
        ICD-10-CM Diagnosis Code H18.54

        Lattice corneal dystrophy

          2016 2017 2018 2019 2020 Billable/Specific Code
      • macular H18.55
        ICD-10-CM Diagnosis Code H18.55

        Macular corneal dystrophy

          2016 2017 2018 2019 2020 Billable/Specific Code
      • specified type NEC H18.59
        ICD-10-CM Diagnosis Code H18.59

        Other hereditary corneal dystrophies

          2016 2017 2018 2019 2020 Billable/Specific Code
    • Duchenne's type G71.01
      ICD-10-CM Diagnosis Code G71.01

      Duchenne or Becker muscular dystrophy

        2019 - New Code 2020 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 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 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 Billable/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 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 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 Billable/Specific Code
    • Landouzy-Déjérine G71.02
      ICD-10-CM Diagnosis Code G71.02

      Facioscapulohumeral muscular dystrophy

        2019 - New Code 2020 Billable/Specific Code
      Applicable To
      • Scapulohumeral muscular dystrophy
    • Leyden-Möbius G71.09
      ICD-10-CM Diagnosis Code G71.09

      Other specified muscular dystrophies

        2019 - New Code 2020 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
      • Limb-girdle muscular dystrophy
      • Ocular muscular dystrophy
      • Oculopharyngeal muscular dystrophy
      • Scapuloperoneal muscular dystrophy
    • muscular G71.00
      ICD-10-CM Diagnosis Code G71.00

      Muscular dystrophy, unspecified

        2019 - New Code 2020 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 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 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 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
          • Limb-girdle 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 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
        • Limb-girdle 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 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 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
        • Limb-girdle 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 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 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
        • Limb-girdle 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 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 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 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)
        ICD-10-CM Diagnosis Code G71.09

        Other specified muscular dystrophies

          2019 - New Code 2020 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
        • Limb-girdle 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 Billable/Specific Code
        Applicable To
        • Scapulohumeral muscular dystrophy
      • limb-girdle G71.09
        ICD-10-CM Diagnosis Code G71.09

        Other specified muscular dystrophies

          2019 - New Code 2020 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
        • Limb-girdle 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 Billable/Specific Code
        Applicable To
        • Dystrophia myotonica [Steinert]
        • Myotonia atrophica
        • Myotonic dystrophy
        • Proximal myotonic myopathy (PROMM)
        • Steinert disease
      • progressive (hereditary) G71.09
        ICD-10-CM Diagnosis Code G71.09

        Other specified muscular dystrophies

          2019 - New Code 2020 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
        • Limb-girdle 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 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 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 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 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
        • Limb-girdle 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 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 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
        • Limb-girdle 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 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 Billable/Specific Code
      • congenital Q84.6
        ICD-10-CM Diagnosis Code Q84.6

        Other congenital malformations of nails

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

          Lipid storage disorder, unspecified

            2016 2017 2018 2019 2020 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 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 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 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 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 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
      • Limb-girdle 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 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 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 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 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 Billable/Specific Code
      • congenital Q84.6
        ICD-10-CM Diagnosis Code Q84.6

        Other congenital malformations of nails

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

      Leukoplakia of vulva

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Dystrophy of vulva
      • Kraurosis of vulva
      • Lichen sclerosus of external female genital organs
    • yellow (liver) - see Failure, hepatic