E79.82

Hereditary xanthinuria

Billable / specific

E79.82 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Inclusion terms

Note: All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.

Not coded here — never report together with this code.

transitory endocrine and metabolic disorders specific to newborn (P70-P74) (from E79)
androgen insensitivity syndrome (E34.5-) (from E79)
congenital adrenal hyperplasia (E25.0) (from E79)
hemolytic anemias attributable to enzyme disorders (D55.-) (from E79)
Marfan syndrome (Q87.4-) (from E79)
5-alpha-reductase deficiency (E29.1) (from E79)
Ataxia-telangiectasia (Q87.19) (from E79)
Bloom's syndrome (Q82.8) (from E79)
Cockayne's syndrome (Q87.19) (from E79)
calculus of kidney (N20.0) (from E79)
combined immunodeficiency disorders (D81.-) (from E79)
Fanconi's anemia (D61.09) (from E79)
gout (M1A.-, M10.-) (from E79)
orotaciduric anemia (D53.0) (from E79)
progeria (E34.8) (from E79)
Werner's syndrome (E34.8) (from E79)
xeroderma pigmentosum (Q82.1) (from E79)

Not included here — may be reported together when both conditions exist.