Home > 2009 ICD-9-CM Diagnosis Codes > Diseases Of The Skin And Subcutaneous Tissue 680-709 > Other Diseases Of Skin And Subcutaneous Tissue 700-709 > Other disorders of skin and subcutaneous tissue 709-
2009 ICD-9-CM Diagnosis Code 709.09
Other dyschromia
- ICD-9-CM 709.09 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
- You are viewing the 2009 version of ICD-9-CM 709.09.
- More recent version(s) of ICD-9-CM 709.09: 2010 2011 2012 2013.
709.09 Alternative Terminology
- 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
- Caf� au lait spot
- Caf�-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 caf�-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 acth/msh-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 acth/msh-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 puva
- Lentigo
- Lentigo - freckle
- Lentigo simplex
- Leukoderma estivale
- 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 caf�-au-lait macules due to neurofibromatosis
- Multiple lentigines 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 due to bismuth
- Pigmentation due to topically applied medicament
- 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
- Unilateral acquired lentiginosis
- Unilateral lentiginosis
- Universal acquired melanosis
- Vulvovaginal hypermelanosis
- Yellow skin
Convert 709.09 to ICD-10-CM 
ICD-9-CM 709.09 converts approximately to:
- 2013 ICD-10-CM L81.8 Other specified disorders of pigmentation
ICD-9-CM Volume 2 Index entries containing back-references to 709.09:
- Anomaly, anomalous (congenital) (unspecified type) 759.9
- Argyria, argyriasis NEC 985.8
from drug or medicinal agent
correct substance properly administered 709.09- overdose or wrong substance given or taken 961.2
- Arsenical
- Atrophia - see also Atrophy
- alba 709.09
- Café au lait spots 709.09
- Chloasma 709.09
- cachecticorum 709.09
- 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
- 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
- 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
- Leukodermia (see also Leukoderma) 709.09
- Mark
- tattoo 709.09
- Melanoderma, melanodermia 709.09
- Addison's (primary adrenal insufficiency) 255.41
- Melanosis 709.09
- adrenal 255.41
- colon 569.89
- corii degenerativa 757.33
- cornea (presenile) (senile) 371.12
- 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
- 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
- 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
- café au lait 709.09
- liver 709.09
- Sutton's disease 709.09
- Tattoo (mark) 709.09
- Xanthosis 709.09
- surgical 998.81
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 709.09 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2009 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
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