Xanthoma (s), xanthomatosis (primary) (familial) (hereditary) - in the ICD-10-CM Index

Browse the ICD-10-CM codes with references applicable to the clinical term "xanthoma (s), xanthomatosis (primary) (familial) (hereditary)"

• Xanthoma (s), xanthomatosis (primary) (familial) (hereditary) - E75.5 Other lipid storage disorders

  • bone (generalisata) - C96.5 Multifocal and unisystemic Langerhans-cell histiocytosis

  • cerebrotendinous - E75.5 Other lipid storage disorders

  • cutaneotendinous - E75.5 Other lipid storage disorders

  • disseminatum (skin) - E78.2 Mixed hyperlipidemia

  • eruptive - E78.2 Mixed hyperlipidemia

  • hypercholesterinemic - E78.00 Pure hypercholesterolemia, unspecified

  • hypercholesterolemic - E78.00 Pure hypercholesterolemia, unspecified

  • hyperlipidemic - E78.5 Hyperlipidemia, unspecified

  • joint - E75.5 Other lipid storage disorders

  • multiple (skin) - E78.2 Mixed hyperlipidemia

  • tendon (sheath) - E75.5 Other lipid storage disorders

  • tuberosum - E78.2 Mixed hyperlipidemia

  • tuberous - E78.2 Mixed hyperlipidemia

  • tubo-eruptive - E78.2 Mixed hyperlipidemia

  • verrucous, oral mucosa - K13.4 Granuloma and granuloma-like lesions of oral mucosa

  • with

    • hyperlipoproteinemia

      • Type I - E78.3 Hyperchylomicronemia

      • Type III - E78.2 Mixed hyperlipidemia

      • Type IV - E78.1 Pure hyperglyceridemia

      • Type V - E78.3 Hyperchylomicronemia

Joints: Also known as articulations, these are points of connection between the ends of certain separate bones, or where the borders of other bones are juxtaposed.