Specific code 2011 ICD-9-CM Diagnosis Code 757.33
Congenital pigmentary anomalies of skin
  • Short description: Cong skin pigment anomal.
  • ICD-9-CM 757.33 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 757.33 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
  • You are viewing the 2011 version of ICD-9-CM 757.33.
  • More recent version(s) of ICD-9-CM 757.33: 2012 2013 2014 2015.
Convert to ICD-10-CM: 757.33 converts approximately to:
  • 2015/16 ICD-10-CM Q82.1 Xeroderma pigmentosum
    Or:
  • 2015/16 ICD-10-CM Q82.2 Mastocytosis
Approximate Synonyms
  • Anomaly of skin pigment, congenital
  • Congenital anomaly of skin pigment
  • Congenital pigmentary skin anomalies
  • Incontinentia pigmenti syndrome
  • Mongolian spot
  • Mongolian spot (blue/gray skin discoloration)
  • Urticaria pigmentosa
  • Xeroderma pigmentosum
757.33 Excludes
Applies To
  • Congenital poikiloderma
  • Urticaria pigmentosa
  • Xeroderma pigmentosum
ICD-9-CM Volume 2 Index entries containing back-references to 757.33:
  • Angioma (M9120/0) (see also Hemangioma, by site) 228.00
    • pigmentosum et atrophicum 757.33
  • Anomaly, anomalous (congenital) (unspecified type) 759.9
  • Asboe-Hansen's disease (incontinentia pigmenti) 757.33
  • Atrophoderma, atrophodermia 701.9
    • pigmentosum 757.33
  • Bloch-Siemens syndrome (incontinentia pigmenti) 757.33
  • Bloch-Stauffer dyshormonal dermatosis 757.33
  • Bloch-Sulzberger disease or syndrome (incontinentia pigmenti) (melanoblastosis) 757.33
  • Chloasma 709.09
  • Dermatosis 709.9
  • Disease, diseased - see also Syndrome
    • Asboe-Hansen's (incontinentia pigmenti) 757.33
    • Bloch-Sulzberger (incontinentia pigmenti) 757.33
    • xeroderma pigmentosum 757.33
    • mast cell 757.33
    • Nettleship's (urticaria pigmentosa) 757.33
    • Thomson's (congenital poikiloderma) 757.33
  • Incontinentia pigmenti 757.33
  • Kaposi's
    • xeroderma pigmentosum 757.33
  • Lioderma essentialis (cum melanosis et telangiectasia) 757.33
  • Mast cell
    • disease 757.33
  • Mastocytosis 757.33
    • malignant (M9741/3) 202.6
  • Melanoblastosis
    • Block-Sulzberger 757.33
    • cutis linearis sive systematisata 757.33
  • Melanosis 709.09
    • corii degenerativa 757.33
    • lenticularis progressiva 757.33
  • Mongolian, mongolianism, mongolism, mongoloid 758.0
    • spot 757.33
  • Naegeli's
    • syndrome (incontinentia pigmenti) 757.33
  • Nettleship's disease (urticaria pigmentosa) 757.33
  • Nevus (M8720/0) - see also Neoplasm, skin, benign
    • comedonicus 757.33
    • pigmented (M8720/0)
      • giant (M8761/1) - see also Neoplasm, skin, uncertain behavior
        • malignant melanoma in (M8761/3) - see Melanoma
      • systematicus 757.33
    • unius lateris 757.33
    • verrucous 757.33
  • Pigmentation (abnormal) 709.00
    • lids (congenital) 757.33
    • scrotum, congenital 757.33
  • Poikiloderma 709.09
    • congenital 757.33
  • Rothmund (-Thomson) syndrome 757.33
  • Spots, spotting
    • Mongolian (pigmented) 757.33
  • Syndrome - see also Disease
    • Block-Siemens (incontinentia pigmenti) 757.33
    • Bloch-Sulzberger (incontinentia pigmenti) 757.33
    • mastocytosis 757.33
    • Rothmund's (congenital poikiloderma) 757.33
    • telangiectasis-pigmentation-cataract 757.33
  • Thomson's disease (congenital poikiloderma) 757.33
  • Urticaria 708.9
    • pigmentosa 757.33
  • Xanthelasmoidea 757.33
  • Xeroderma (congenital) 757.39
    • pigmentosum 757.33
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 757.33 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 2011 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.