Diagnosis Code: 709.09

Short Description: Other dyschromia

Long Description: Other dyschromia

Code Classification:

• Diseases of the skin and subcutaneous tissue (680–709)
  • Other diseases of skin and subcutaneous tissue (700-709)
    • 709 Other disorders of skin and subcutaneous tissue
      • 709.09 Other dyschromia

Code Version: 2015 ICD-9-CM

Synonyms

• Accidental and/or traumatic tattoo
• Achromia of skin
• Acquired hypermelanotic disorder
• Acquired hypomelanosis of uncertain etiology
• Acquired poikiloderma
• Acromelanosis
• Addisonian pigmentation of palms
• Amateur decorative tattoo of skin
• Arsenic-induced skin pigmentation
• Atrial myxoma with lentigines
• Axillary freckling due to neurofibromatosis
• Bilirubin pigmentation of oral mucosa
• Breast depigmented
• Breast hypopigmented
• Buccal pigmentation due to Addison's disease
• Café au lait spot
• Café-au-lait spots and ring chromosome 11
• Centrofacial lentiginosis syndrome
• Chemically-induced hypomelanosis
• Chloasma
• Chloasma bronzinum
• Chloasma cachecticorum
• Chloasma caloricum
• Chloasma hepaticum
• Chloasma toxicum
• Chloasma traumaticum
• Chlorpromazine pigmentation
• Circumscribed acquired hypermelanosis
• Circumscribed hypermelanosis
• Circumscribed hypomelanosis
• Collier's stripes
• Congenital/hereditary hypermelanotic disorder
• Congenital/hereditary lentiginosis
• Crystal violet tattoo
• Decorative tattoo of skin
• Drug-induced hypermelanosis
• Drug-induced melasma
• Drug-induced pigmentation
• Ephelides
• Ephelis
• Eruptive lentiginosis
• Familial multiple café-au-lait macules without neurofibromatosis
• Generalized acquired lentiginosis
• Generalized lentiginosis
• Genital lentiginosis
• Halo nevus
• Hemosiderin pigmentation of skin
• Hereditary diffuse melanosis
• Hereditary reticulate melanosis
• Hereditary sclerosing poikiloderma
• Hereditary sclerosing poikiloderma of Weary
• Hypermelanosis due to acromegaly
• Hypermelanosis due to adrenocorticotropic hormone/melanocyte stimulating hormone-secreting tumor
• Hypermelanosis due to connective tissue disorder
• Hypermelanosis due to cryotherapy
• Hypermelanosis due to Cushing syndrome
• Hypermelanosis due to endocrine disorder
• Hypermelanosis due to Hodgkin's disease
• Hypermelanosis due to hormonal factor
• Hypermelanosis due to hyperthyroidism
• Hypermelanosis due to malignant adrenocorticotropic hormone/melanocyte stimulating hormone-secreting tumor
• Hypermelanosis due to neoplasia
• Hypermelanosis due to nervous system disorder
• Hypermelanosis due to nutritional disorder
• Hypermelanosis due to pheochromocytoma
• Hypermelanosis due to photodynamic agent
• Hypermelanosis due to phytophotodermatitis
• Hypermelanosis following phototherapy for neonatal jaundice
• Hypermelanosis of the eyelids due to hyperthyroidism
• Hypermelanosis of undetermined etiology
• Hyperpigmentation of skin
• Hypomelanosis due to cryotherapy
• Hypomelanosis due to scarring
• Hypomelanosis surrounding malignant melanoma
• Iatrogenic tattoo
• Idiopathic chloasma
• Idiopathic guttate hypomelanosis
• Inherited cutaneous hyperpigmentation
• Iron pigmentation of oral mucosa
• Iron salt tattoo
• Labial lentigo
• Lentiginosis due to psoralen and long-wave ultraviolet radiation therapy
• Lentigo
• Lentigo - freckle
• Lentigo simplex
• Leukoderma estivale
• Local exogenous pigmentation of oral soft tissue
• Lupus erythematosus-associated hypermelanosis
• Lupus erythematosus-associated poikiloderma
• Melanin pigmentation of oral mucosa
• Melanoderma
• Melanoderma cachecticorum
• Melanodermatitis toxica lichenoides
• Melanosis
• Melanosis of vulva
• Mercury pigmentation of skin
• Mucosal lentiginosis
• Multiple café-au-lait macules due to neurofibromatosis
• Multiple lentigines syndrome
• Neurofibromatosis type 1-like syndrome
• Nevoid acquired lentiginosis
• Nevoid lentiginosis
• Nevus anemicus
• Occupational tattoo
• Oral melanocytic macule
• Oral pigmentary incontinence
• Parasitic melanoderma
• Penile hypermelanosis
• Periorbital hypermelanosis
• Phylloid hypomelanosis
• Pigmentary incontinence
• Pigmentation
• Pigmentation due to bismuth
• Pigmented peribuccal erythrosis of Brocq
• Pinna depigmented
• Pinna hypopigmented
• Poikiloderma
• Poikiloderma due to cold injury
• Poikiloderma due to connective tissue disease
• Poikiloderma due to heat of infra-red radiation
• Poikiloderma due to lichen planus
• Poikiloderma due to photodynamic agent
• Poikiloderma of Civatte
• Poikilodermatous mycosis fungoides
• Port-wine stain with oculocutaneous melanosis
• Post-infective hypomelanosis
• Postinflammatory skin pigmentation change
• Presence of xanthochromia
• Professional decorative tattoo of skin
• Progressive pigmentary dermatosis
• Progressive pigmentary dermatosis of Schamberg
• Reticulate acropigmentation of Kitamura
• Riehl's melanosis
• Scleroderma-associated hypermelanosis
• Scleroderma-associated poikiloderma
• Senile lentigo
• Senile melanoderma
• Skin pigmentation due to hemosiderosis
• Solar lentiginosis
• Staining of skin
• Symmetrical progressive leucopathy
• Symptomatic chloasma
• Systemic exogenous pigmentation of oral mucosa
• Tattoo of skin
• Unilateral acquired lentiginosis
• Unilateral lentiginosis
• Universal acquired melanosis
• Vulvovaginal hypermelanosis
• Yellow skin

References to Index of Diseases and Injuries

The code 709.09 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Anomaly, anomalous (congenital) (unspecified type) 759.9
  • pigmentation 709.00
    • specified NEC 709.09

• Argyria, argyriasis NEC 985.8
  • from drug or medicinal agent
    • correct substance properly administered 709.09

• Arsenical
  • pigmentation 985.1
    • from drug or medicinal agent
      • correct substance properly administered 709.09

• Atrophia - see also Atrophy
  • alba 709.09

• Caf� au lait spots 709.09

• Chloasma 709.09
  • cachecticorum 709.09
  • eyelid 374.52
    • congenital 757.33
    • hyperthyroid 242.0
  • gravidarum 646.8
  • idiopathic 709.09
  • skin 709.09
  • symptomatic 709.09

• Civatte's disease or poikiloderma 709.09

• Dermatitis (allergic) (contact) (occupational) (venenata) 692.9
  • Schamberg's (progressive pigmentary dermatosis) 709.09

• Dermatosis 709.9
  • pigmentary NEC 709.00
    • progressive 709.09
    • Schamberg's 709.09
  • progressive pigmentary 709.09
  • Schamberg's (progressive pigmentary) 709.09

• Disease, diseased - see also Syndrome
  • Civatte's (poikiloderma) 709.09
  • Schamberg's (progressive pigmentary dermatosis) 709.09
  • Sutton's 709.09

• Ephelides, ephelis 709.09

• Freckle 709.09
  • malignant melanoma in (M8742/3) - see Melanoma
  • melanotic (of Hutchinson) (M8742/2) - see Neoplasm, skin, in situ
  • retinal 239.81

• Lentigo (congenital) 709.09
  • juvenile 709.09
  • Maligna (M8742/2) - see also Neoplasm, skin, in situ
    • melanoma (M8742/3) - see Melanoma
  • senile 709.09

• Leukoderma 709.09
  • syphilitic 091.3
    • late 095.8

• Leukodermia (see also Leukoderma) 709.09

• Mark
  • tattoo 709.09

• Melanoderma, melanodermia 709.09
  • Addison's (primary adrenal insufficiency) 255.41

• Melanosis 709.09
  • addisonian (primary adrenal insufficiency) 255.41
    • tuberculous (see also Tuberculosis) 017.6
  • adrenal 255.41
  • colon 569.89
  • conjunctiva 372.55
    • congenital 743.49
  • corii degenerativa 757.33
  • cornea (presenile) (senile) 371.12
    • congenital 743.43
      • interfering with vision 743.42
    • prenatal 743.43
      • interfering with vision 743.42
  • eye 372.55
    • congenital 743.49
  • jute spinners' 709.09
  • lenticularis progressiva 757.33
  • liver 573.8
  • precancerous (M8741/2) - see also Neoplasm, skin, in situ
    • malignant melanoma in (M8741/3) - see Melanoma
  • Riehl's 709.09
  • sclera 379.19
    • congenital 743.47
  • suprarenal 255.41
  • tar 709.09
  • toxic 709.09

• Melasma 709.09
  • adrenal (gland) 255.41
  • suprarenal (gland) 255.41

• Nevus (M8720/0) - see also Neoplasm, skin, benign
  • anemic, anemicus 709.09
  • avasculosus 709.09

• Piebaldism, classic 709.09

• Pigmentation (abnormal) 709.00
  • anomalies NEC 709.00
    • specified NEC 709.09

• Poikiloderma 709.09
  • Civatte's 709.09
  • congenital 757.33
  • vasculare atrophicans 696.2

• Purpura 287.2
  • pigmentaria, progressiva 709.09

• Riehl's melanosis 709.09

• Schamberg's disease, dermatitis, or dermatosis (progressive pigmentary dermatosis) 709.09

• Spots, spotting
  • caf� au lait 709.09
  • liver 709.09

• Sutton's disease 709.09

• Tattoo (mark) 709.09

• Xanthosis 709.09
  • surgical 998.81

Crosswalk Information

The code 709.09 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

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