AutoICD API

D69.42

Billable

Congenital and hereditary thrombocytopenia purpura

Congenital and hereditary thrombocytopenia purpura

Status

Billable / Specific

Block

D65-D69

Parent Code

D69.4

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Congenital thrombocytopenia
  • Hereditary thrombocytopenia

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Code First

The underlying condition must be sequenced before this code

Related Codes(2)
D69.41

Evans syndrome

BillableD69.49

Other primary thrombocytopenia

Billable
Also Known As / Clinical Terms(133)

SNOMED CT

UMLS

Clinical Terms

  • Congenital ADAMTS-13 deficiency
  • Giant platelet syndrome
  • Severe autosomal recessive macrothrombocytopenia
  • GATA binding protein 1 related thrombocytopenia with dyserythropoiesis
  • Bleeding diathesis due to thromboxane synthesis deficiency
  • GATA 1 related cytopenia
  • X-linked congenital dyserythropoietic anaemia with thrombocytopenia
  • TTP - thrombotic thrombocytopenic purpura
  • Cutaneovisceral angiomatosis, thrombocytopenia syndrome
  • X linked macrothrombocytopenia
  • Congenital dyserythropoietic anemia
  • Amegakaryocytic thrombocytopenia
  • Moschowitz's syndrome
  • Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome
  • Hereditary thrombocytopenia with early-onset myelofibrosis
  • ATRUS syndrome
  • DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
  • Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome
  • CDA - congenital dyserythropoietic anaemia
  • MYH9-related syndromic thrombocytopenia
  • Congenital autosomal recessive small-platelet thrombocytopenia
  • Platelet secretory disorder
  • CARST - congenital autosomal recessive small-platelet thrombocytopenia
  • Secondary thrombocytopenia
  • Dyserythropoietic anemia and thrombocytopenia
  • Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
  • Congenital dyserythropoietic anaemia
  • Megakaryocytic thrombocytopenia
  • Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome
  • Congenital thrombocytopaenia
  • Familial TTP/HUS
  • Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome
  • Upshaw-Schulman syndrome
  • thrombocytopenia, congenital
  • Congenital radioulnar synostosis
  • Secretion defect of platelets
  • Thrombotic thrombocytopenic purpura
  • Sex-linked thrombocytopenia
  • X-linked thrombocytopenia with normal platelets
  • Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome
  • Autosomal dominant macrothrombocytopenia
  • Amegakaryocytic thrombocytopenia with congenital malformation
  • MYH9 related disease
  • Congenital thrombocytopenia (disorder)
  • Hereditary thrombocytopenia
  • X-linked thrombocytopaenia with normal platelets
  • Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome
  • CDA - congenital dyserythropoietic anemia
  • DIAPH1-related sensorineural deafness, thrombocytopenia syndrome
  • Takenouchi Kosaki syndrome
  • Hereditary thrombocytopenic disorder
  • MLT - multifocal lymphangioendotheliomatosis with thrombocytopenia
  • Beta thalassaemia X-linked thrombocytopenia syndrome
  • Moschcowitz syndrome
  • Dyserythropoietic anaemia and thrombocytopaenia
  • GATA 1 related X linked cytopenia
  • Congenital thrombocytopenia
  • GATA binding protein 1 related thrombocytopaenia with dyserythropoiesis
  • Hereditary thrombocytopenia with normal platelets
  • Congenital amegakaryocytic thrombocytopenia
  • Myosin heavy chain 9 non muscle related disease
  • Autosomal dominant thrombocytopenia with platelet secretion defect
  • Beta thalassemia X-linked thrombocytopenia syndrome
  • X-linked congenital dyserythropoietic anemia with thrombocytopenia
Frequently Asked Questions
What is the ICD-10 code for congenital and hereditary thrombocytopenia purpura?

The ICD-10-CM code for congenital and hereditary thrombocytopenia purpura is D69.42. The full clinical description is "Congenital and hereditary thrombocytopenia purpura". D69.42 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D69.42 mean?

ICD-10-CM code D69.42 represents “Congenital and hereditary thrombocytopenia purpura”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.

Is D69.42 a billable code?

Yes, D69.42 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D69.42 in?

D69.42 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D69.42?

D69.42 has Excludes1 notes indicating codes that cannot be used together with it, including: benign hypergammaglobulinemic purpura (D89.0); cryoglobulinemic purpura (D89.1); essential (hemorrhagic) thrombocythemia (D47.3); and 6 more.

What SNOMED CT codes does D69.42 map to?

D69.42 maps to 30 SNOMED CT concepts: 721882001, 234482009, 359531004, 720521008, 1187252002, and 25 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D69.42?

D69.42 is linked to 2 UMLS Concept Unique Identifiers: C2873807, C0272278. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D69.42 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital and hereditary thrombocytopenia purpura affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of D69.42?

There is no direct ICD-11 mapping available for D69.42 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.