ICD-10-CM Xanthoma (s), xanthomatosis (primary) (familial) (hereditary) References

"Xanthoma (s), xanthomatosis (primary) (familial) (hereditary)" Annotation Back-References in the ICD-10-CM Index to Diseases and Injuries

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

Applicable Clinical Terms Definitions

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.