Diagnosis Code: 757.33

Short Description: Cong skin pigment anomal

Long Description: Congenital pigmentary anomalies of skin

Code Classification:

• Congenital anomalies (740–759)
  • Congenital anomalies (740-759)
    • 757 Congenital anomalies of the integument
      • 757.33 Cong skin pigment anomal

Code Version: 2015 ICD-9-CM

References to Index of Diseases and Injuries

The code 757.33 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Angioma (M9120/0) (see also Hemangioma, by site) 228.00
  • pigmentosum et atrophicum 757.33

• Anomaly, anomalous (congenital) (unspecified type) 759.9
  • pigmentation 709.00
    • congenital 757.33

• 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
  • eyelid 374.52
    • congenital 757.33

• Dermatosis 709.9
  • pigmentary NEC 709.00
    • Siemens-Bloch 757.33

• Disease, diseased - see also Syndrome
  • Asboe-Hansen's (incontinentia pigmenti) 757.33
  • Bloch-Sulzberger (incontinentia pigmenti) 757.33
  • Kaposi's 757.33
    • lichen ruber 697.8
      • acuminatus 696.4
      • moniliformis 697.8
  • xeroderma pigmentosum 757.33
  • mast cell 757.33
    • systemic (M9741/3) 202.6
  • Nettleship's (urticaria pigmentosa) 757.33
  • Thomson's (congenital poikiloderma) 757.33

• Incontinentia pigmenti 757.33

• Kaposi's
  • disease 757.33
    • lichen ruber 696.4
      • acuminatus 696.4
      • moniliformis 697.8
  • xeroderma pigmentosum 757.33

• Lioderma essentialis (cum melanosis et telangiectasia) 757.33

• Mast cell
  • disease 757.33
    • systemic (M9741/3) 202.6

• Mastocytosis 757.33
  • malignant (M9741/3) 202.6
  • systemic (M9741/3) 202.6

• Melanoblastosis
  • Block-Sulzberger 757.33
  • cutis linearis sive systematisata 757.33

• Melanocytosis, neurocutaneous 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)
    • systematicus 757.33
  • unius lateris 757.33
  • verrucous 757.33

• Pigmentation (abnormal) 709.00
  • anomalies NEC 709.00
    • congenital 757.33
  • lids (congenital) 757.33
    • acquired 374.52
  • 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

Crosswalk Information

The code 757.33 converts into the following ICD-10 code(s):

Similar Codes

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

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