Diagnosis Code: D69.42

Short Description: Congenital and hereditary thrombocytopenia purpura

Long Description: Congenital and hereditary thrombocytopenia purpura

The code D69.42 is VALID for claim submission

Code Classification:

• Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
  • Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
    • Purpura and other hemorrhagic conditions (D69)
      • D69.42 Congenital and hereditary thrombocytopenia purpura

Code Version: 2022 ICD-10-CM

Synonyms

• Amegakaryocytic thrombocytopenia
• Amegakaryocytic thrombocytopenia
• Amegakaryocytic thrombocytopenia
• Amegakaryocytic thrombocytopenia with congenital malformation
• Amegakaryocytic thrombocytopenia with congenital malformation
• Autosomal dominant macrothrombocytopenia
• Autosomal dominant thrombocytopenia with platelet secretion defect
• Beta thalassemia X-linked thrombocytopenia syndrome
• Bleeding diathesis due to thromboxane synthesis deficiency
• Congenital amegakaryocytic thrombocytopenia
• Congenital autosomal recessive small-platelet thrombocytopenia
• Congenital dyserythropoietic anemia
• Congenital thrombocytopenia
• DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
• GATA binding protein 1 related thrombocytopenia with dyserythropoiesis
• Giant platelet syndrome
• Giant platelet syndrome
• Hereditary thrombocytopenia with early-onset myelofibrosis
• Hereditary thrombocytopenia with normal platelets
• Hereditary thrombocytopenic disorder
• Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
• Megakaryocytic thrombocytopenia
• Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome
• MYH9 related disease
• Platelet secretory disorder
• Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome
• Secondary thrombocytopenia
• Severe autosomal recessive macrothrombocytopenia
• Sex-linked thrombocytopenia
• Thrombotic microangiopathy
• Thrombotic thrombocytopenic purpura
• Upshaw-Schulman syndrome
• X-linked congenital dyserythropoietic anemia with thrombocytopenia
• X-linked thrombocytopenia with normal platelets

References to Index of Diseases and Injuries

The code D69.42 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital thrombocytopenia
  • Hereditary thrombocytopenia
• Code First:
  • congential or hereditary disorder, such as:
  • thrombocytopenia with absent radius (TAR syndrome) (@Q87.2*)

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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