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
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
- Kaposi's 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
- disease 757.33
- 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