Kodex

ICD-10-CM-TERMS

Term

familial lecithin cholesterol acyltransferase deficiency

Hierarchy

Disorder (of)
- glomerular (in)
  - amyloidosis
  - cryoglobulinemia
  - disseminated intravascular coagulation
  - Fabry's disease
  - familial lecithin cholesterol acyltransferase deficiency
  - Goodpasture's syndrome
  - hemolytic-uremic syndrome
  - Henoch purpura (-Schönlein)
  - malariae malaria
  - microscopic polyangiitis
  - multiple myeloma
  - mumps
  - schistosomiasis
  - sepsis NEC
  - sickle-cell disorders
  - strongyloidiasis
  - subacute bacterial endocarditis
  - syphilis
  - systemic lupus erythematosus
  - thrombotic thrombocytopenic purpura
  - Waldenström macroglobulinemia
  - Wegener's granulomatosis

Long Title

familial lecithin cholesterol acyltransferase deficiency

Disorder (of) glomerular (in) familial lecithin cholesterol acyltransferase deficiency

Codes

E78.6 Lipoprotein deficiency

N08 Glomerular disorders in diseases classified elsewhere