Category · FY2027
D50 Iron deficiency anemia
- Header · not billable
D50 is not billable. The category heads 4 billable codes in FY2027: the 4 codes directly below it.
Index → code
Where it sits
- Billable codes
- 4
- Subdivisions
- 4
- CC / MCC codes
- 0 / 0
- HCC V28 codes
- 0
- New FY2027
- 0
- Index entries
- 61
Codes in D50
- D50.0
- D50.1Sideropenic dysphagiaBillable
Inclusion terms 2
Inclusion terms
- Kelly-Paterson syndrome
- Plummer-Vinson syndrome
- D50.8Other iron deficiency anemiasBillable
Inclusion terms 1
Inclusion terms
- Iron deficiency anemia due to inadequate dietary iron intake
- D50.9Iron deficiency anemia, unspecifiedBillable
Instructions
At D50
Includes
- asiderotic anemia
- hypochromic anemia
Notes that also apply
Chapter 3 instructions (Excludes2 9): printed on the chapter 3 page.
Index entries
- Normocytic anemia (infectional) due to blood loss (chronic) → D50.0
- Posthemorrhagic anemia (chronic) → D50.0
- Kelly (-Patterson) syndrome (sideropenic dysphagia) → D50.1
- Paterson (-Brown)(-Kelly) syndrome or web → D50.1
- Plummer-Vinson syndrome → D50.1
- Vinson-Plummer syndrome → D50.1
- Waldenström-Kjellberg syndrome → D50.1
- Chlorotic anemia → D50.8
- Green sickness → D50.8
- Hypochromasia, blood cells → D50.8
- Witts' anemia → D50.8
- Chlorosis → D50.9
- Faber's syndrome (achlorhydric anemia) → D50.9
- Hyposiderinemia → D50.9
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›blood loss (chronic) → D50.0
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›factitious (self-induced blood letting) → D50.0
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›hemorrhagic (chronic) → D50.0
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›posthemorrhagic (chronic) → D50.0
- Hemorrhage, hemorrhagic (concealed)›anemia (chronic) → D50.0
- Dysphagia›sideropenic → D50.1
- Syndrome›Kelly's → D50.1
- Syndrome›Paterson (-Brown) (-Kelly) → D50.1
- Syndrome›Plummer-Vinson → D50.1
- Syndrome›sideropenic → D50.1
- Syndrome›Vinson-Plummer → D50.1
- Syndrome›Waldenström-Kjellberg → D50.1
- Web, webbed (congenital)›Paterson-Kelly → D50.1
- Achlorhydria, achlorhydric (neurogenic)›anemia → D50.8
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›achlorhydric → D50.8
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›chlorotic → D50.8
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›Witts' (achlorhydric anemia) → D50.8
- Sickness›green → D50.8
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›asiderotic → D50.9
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›Faber's (achlorhydric anemia) → D50.9
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›hypochromic (idiopathic) (microcytic) (normoblastic) → D50.9
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›iron deficiency → D50.9
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›microcytic (hypochromic) → D50.9
- Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)›sideropenic (refractory) → D50.9
- Syndrome›Faber's → D50.9
- Syndrome›Hayem-Faber → D50.9
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