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Q82.3

Billable

Incontinentia pigmenti

This code does not map to an HCC category in any model (V28, V24, ESRD, RxHCC).

What This Code Means

A rare inherited skin disorder characterized by abnormal pigmentation patterns that typically appear in lines or whorls on the skin, usually affecting females.

Coding Tips

  • •This condition is X-linked dominant; document family history if available
  • •May be associated with other congenital anomalies; code additional conditions separately

Code Hierarchy

└Q82Other congenital malformations of skin└Q82.3Incontinentia pigmenti
└Q82.3Incontinentia pigmenti

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