Alphabetic Index · main term
Leukomelanopathy, hereditary
Leukomelanopathy, hereditary is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists D72.0 for this term: Genetic anomalies of leukocytes. It is a billable code. Confirm any code you find here in the Tabular List before you report it.
Code the Index gives
Genetic anomalies of leukocytes
Other Index terms that lead to D72.0
Different words, same code. 25 entries
- Alder (-Reilly) anomaly or syndrome (leukocyte granulation)
- Anomaly, anomalous (congenital) (unspecified type), Alder (-Reilly) (leukocyte granulation)
- Anomaly, anomalous (congenital) (unspecified type), granulation or granulocyte, genetic (constitutional) (leukocyte)
- Anomaly, anomalous (congenital) (unspecified type), Hegglin's
- Anomaly, anomalous (congenital) (unspecified type), hypersegmentation of neutrophils, hereditary
- Anomaly, anomalous (congenital) (unspecified type), Jordan's
- Anomaly, anomalous (congenital) (unspecified type), leukocytes, genetic
- Anomaly, anomalous (congenital) (unspecified type), leukocytes, genetic, granulation (constitutional)
- Anomaly, anomalous (congenital) (unspecified type), May (-Hegglin)
- Anomaly, anomalous (congenital) (unspecified type), Pelger-Huët (hereditary hyposegmentation)
- Dohle body panmyelopathic syndrome
- Dysgenesis, reticular
Show 13 more
- Hegglin's anomaly or syndrome
- Hypersegmentation, leukocytic, hereditary
- Hyposegmentation, leukocytic, hereditary
- Inclusion, azurophilic leukocytic
- Jordan's anomaly or syndrome
- May (-Hegglin) anomaly or syndrome
- Neutrophilia, hereditary giant
- Pelger-Huët anomaly or syndrome
- Syndrome, Alder's
- Syndrome, Döhle body-panmyelopathic
- Syndrome, Hegglin's
- Syndrome, May (-Hegglin)
- Syndrome, Pelger-Huet