Reserved for future guideline expansion
How to use this page
Everything the published sources say about one code, on one page.
- Read the Excludes1 block first — it is the one that stops you coding this at all alongside another code.
- Excludes2, Code first, Use additional and Includes follow. A note inherited from a parent category is labelled with the category it came from, so you can see why it applies.
- Official Guidelines sit below. "Guidelines naming this code" cite the code or a range containing it; "Chapter guidance" is the general guidance for its chapter and is the weaker signal.
- Guideline text is quoted verbatim with its section number and page, so you can check it against the published document.
- Risk-model chips show which published CMS models map this code.
What this page does not do
- Guidance is quoted, never paraphrased — a paraphrase of a coding rule is a different rule.
- Medication candidates, where shown, are matched by condition *name* and are offered as candidates for you to judge. They are not "the drugs for this code".
Exclusions9never code together
D50-D89chapter
Excludes2
- autoimmune disease (systemic) NOS (M35.9)M35.9
- certain conditions originating in the perinatal period (P00-P96)P00-P96
- complications of pregnancy, childbirth and the puerperium (O00-O9A)O00-O9A
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)Q00-Q99
- endocrine, nutritional and metabolic diseases (E00-E88)E00-E88
- human immunodeficiency virus [HIV] disease (B20)B20
- injury, poisoning and certain other consequences of external causes (S00-T88)S00-T88
- neoplasms (C00-D49)C00-D49
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)R00-R94
Excludes2 — not included here, but the patient may have both. Code both when documented.
Instructional notes
No further instructional notes apply.
Official Guidelines1names this code
ICD-10-CM Official Guidelines for Coding and Reporting, quoted in full. Published by CMS and NCHS; in the public domain.
Index entries leading here5
- Abrami's disease D59.8
- Jaundice (yellow) R17
- acholuric (familial) (splenomegalic) — see also Spherocytosis
- acquired D59.8
- acholuric (familial) (splenomegalic) — see also Spherocytosis
- Acholuric jaundice (familial) (splenomegalic) — see also Spherocytosis
- acquired D59.8
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
- Hayem-Widal syndrome D59.8
Alongside this code8same parent — D59
D59.0 Drug-induced autoimmune hemolytic anemia D59.1 Other autoimmune hemolytic anemias category D59.2 Drug-induced nonautoimmune hemolytic anemia D59.3 Hemolytic-uremic syndrome category D59.4 Other nonautoimmune hemolytic anemias D59.5 Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli] D59.6 Hemoglobinuria due to hemolysis from other external causes D59.9 Acquired hemolytic anemia, unspecified
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.