Diagnosis Code D75.0
Information for Medical Professionals
The diagnosis code D75.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG v33.0)
- RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH MCC 814
- RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITH CC 815
- RETICULOENDOTHELIAL AND IMMUNITY DISORDERS WITHOUT CC/MCC 816
Convert to ICD-9 General Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.
- 289.6 - Familial polycythemia
- Chronic myeloproliferative disorder
- Disorder of manganese metabolism
- Familial erythrocytosis
- Familial erythrocytosis due to diphosphoglycerate mutase deficiency
- Familial polycythemia vera
- Hypermanganesemia with dystonia, polycythemia, and cirrhosis
- Polycythemia vera
Index of Diseases and Injuries
References found for the code D75.0 in the Index of Diseases and Injuries:
- Inclusion Terms: Inclusion terms
List of terms is included under some codes. These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of “other specified” codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- Benign polycythemia
- Familial polycythemia
- Type 1 Excludes Notes: Type 1 Excludes Notes
A type 1 Excludes note is a pure excludes note. It means “NOT CODED HERE!” An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- hereditary ovalocytosis (D58.1)
Information for Patients
Also called: Hematologic diseases
Your blood is living tissue made up of liquid and solids. The liquid part, called plasma, is made of water, salts and protein. Over half of your blood is plasma. The solid part of your blood contains red blood cells, white blood cells and platelets.
Blood disorders affect one or more parts of the blood and prevent your blood from doing its job. They can be acute or chronic. Many blood disorders are inherited. Other causes include other diseases, side effects of medicines, and a lack of certain nutrients in your diet.
Types of blood disorders include
- Platelet disorders, excessive clotting, and bleeding problems, which affect how your blood clots
- Anemia, which happens when your blood does not carry enough oxygen to the rest of your body
- Cancers of the blood, such as leukemia and myeloma
- Eosinophilic disorders, which are problems with one type of white blood cell.
- Blood differential
- Blood smear
- Low white blood cell count and cancer
- RBC count
- RBC indices
- WBC count
Familial erythrocytosis Familial erythrocytosis is an inherited condition characterized by an increased number of red blood cells (erythrocytes). The primary function of these cells is to carry oxygen from the lungs to tissues and organs throughout the body. Signs and symptoms of familial erythrocytosis can include headaches, dizziness, nosebleeds, and shortness of breath. The excess red blood cells also increase the risk of developing abnormal blood clots that can block the flow of blood through arteries and veins. If these clots restrict blood flow to essential organs and tissues (particularly the heart, lungs, or brain), they can cause life-threatening complications such as a heart attack or stroke. However, many people with familial erythrocytosis experience only mild signs and symptoms or never have any problems related to their extra red blood cells.