2007 ICD-9-CM Diagnosis Code 757.33 : Congenital pigmentary anomalies of skin

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2007 ICD-9-CM Diagnosis Code 757.33

Congenital pigmentary anomalies of skin

757.32

757.39

757.33 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.
Newer versions of 757.33: 2008 2009 2010

Diagnosis Definition(s) Click to expand

Excludes

Also applicable to/known as Click to expand

ICD-9-CM Volume 2 Index Entries That Refer To 757.33 Click to expand

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

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

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