D69.1

Billable

Qualitative platelet defects

Qualitative platelet defects

Status

Billable / Specific

Block

D65-D69

Parent Code

D69

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Bernard-Soulier [giant platelet] syndrome
  • Glanzmann's disease
  • Grey platelet syndrome
  • Thromboasthenia (hemorrhagic) (hereditary)
  • Thrombocytopathy

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

Related Codes(8)
D69.0

Allergic purpura

BillableD69.2

Other nonthrombocytopenic purpura

BillableD69.3

Immune thrombocytopenic purpura

BillableD69.4

Other primary thrombocytopenia

D69.5

Secondary thrombocytopenia

D69.6

Thrombocytopenia, unspecified

BillableD69.8

Other specified hemorrhagic conditions

BillableD69.9

Hemorrhagic condition, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

3B62.ZQualitative platelet defects, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(343)

SNOMED CT

UMLS

Clinical Terms

  • Giant platelet syndrome
  • Bleeding disorder due to glycoprotein VI deficiency
  • Platelet Glycoprotein 2b 3a Deficiency
  • Hereditary hemorrhagic thrombasthenia
  • Acquired platelet factor 3 disease
  • Platelet satellite
  • Abnormal platelet destruction
  • Platelet dysfunction associated with uraemia
  • Scott syndrome
  • Glanzmann Thrombasthenia, Type A
  • Megakaryocyte finding
  • BDPLT2
  • Hereditary haemorrhagic thrombasthenia
  • Deficiency of GP 2b 3a Complex
  • Stormorken syndrome
  • Asplenia
  • Platelet Glycoprotein IIb-IIIa Deficiency
  • Glanzmann thrombasthenia
  • Glycoprotein VI deficiency
  • Thrombasthenia
  • Platelet procoagulant activity deficiency
  • Bernard-Soulier [giant platelet] syndrome
  • Autoimmune state
  • Platelet Syndromes, Grey
  • Thromboasthenia (hemorrhagic) (hereditary)
  • Gray Platelet Syndrome
  • Bernard-Soulier syndrome
  • CDA - congenital dyserythropoietic anemia
  • GLANZMANN THROMBASTHENIA 1
  • PLATELET ALPHA-GRANULE DEFICIENCY
  • Glycoprotein Complex IIb IIIa, Deficiency Of
  • Isolated collagen aggregation defect
  • Decreased platelet life span
  • Glycoprotein Complex IIb-IIIa, Deficiency Of
  • Nucleotide storage pool disorder
  • Platelet storage pool defect
  • Platelet alpha granule deficiency
  • Thrombasthenia of Glanzmann and Naegeli
  • Ineffective thrombopoiesis
  • Glycoprotein IIb/IIIa defect
  • Uremic platelet dysfunction
  • X-linked dyserythropoietic anemia with abnormal platelets and neutropenia
  • BDPLT4
  • Syndrome, Grey Platelet
  • Glycoprotein Ia defect
  • Platelet satellitism
  • GT1
  • Glanzmann thromboasthenia
  • Glanzmann's disease
  • Exhausted platelets
  • GLYCOPROTEIN COMPLEX IIb-IIIa DEFICIENCY
  • Autosensitivity
  • GP IIb-IIIa COMPLEX DEFICIENCY
  • Medich macrothrombocytopenia
  • Thrombocytopathy
  • grey platelet syndrome
  • Dense body deficiency
  • Glanzmann's thrombasthenia
  • Platelet membrane defect
  • Platelet secretory disorder
  • Miotic pupil
  • Platelet dysfunction caused by aspirin
  • Sensitized cell
  • Glanzmann disease
  • Congenital dyserythropoietic anaemia
  • Megakaryocytic thrombocytopenia
  • Autoimmunity
  • Platelet sequestration
  • Pupil constriction
  • Platelet disorder
  • Bernard Soulier syndrome
  • Acquired platelet function disorder
  • Increased platelet destruction
  • Gray Platelet Syndromes
  • Platelet clumps
  • Inherited platelet disorder
  • Platelet Fibrinogen Receptor, Deficiency of
  • Decreased platelet destruction
  • Dense body defect
  • Sensitized platelet
  • Thromboxane synthetase deficiency
  • Glanzmann's thrombasthenia (disorder)
  • Autoplatelet sensitivity
  • Qualitative platelet defect
  • Medich giant platelet syndrome
  • BLEEDING DISORDER, PLATELET-TYPE, 2
  • Familial platelet disorder with associated myeloid malignancy
  • Syndromes, Gray Platelet
  • Familial platelet syndrome with predisposition to acute myelogenous leukaemia
  • Hereditary thrombocytopathy
  • Deficient alpha granule syndrome
  • Mixed alpha granule and dense body deficiency
  • Thrombasthenia, Glanzmann
  • Glanzmann's syndrome
  • Cyclooxygenase deficiency
  • Acquired storage pool deficiency (platelets)
  • Acquired platelet disorder
  • Mediterranean macrothrombocytopenia
  • Miosis
  • Hereditary thrombasthenia
  • Platelet dense granule deficiency
  • Glycoprotein Ib defect
  • glanzmanns thrombasthenia
  • Platelet dysfunction associated with uremia
  • Platelet Glycoprotein 2b-3a Deficiency
  • Sensitised platelet
  • Syndrome, Gray Platelet
  • Platelet granule defect
  • Hereditary thromboasthenia
  • Platelet morphology - finding
  • Small pupil
  • Uraemic platelet dysfunction
  • Thrombocytopathy, asplenia and miosis
  • Finding of platelet morphology
  • Bleeding disorder platelet-type 11
  • Grey Platelet Syndromes
  • Deficiency of platelet fibrinogen receptor
  • GP IIb IIIa Complex, Deficiency Of
  • Montreal platelet syndrome
  • Bleeding diathesis due to collagen receptor defect
  • Abnormal platelet production
  • Familial platelet syndrome with predisposition to acute myelogenous leukemia
  • Platelet Glycoprotein IIb IIIa Deficiency
  • Montreal syndrome
  • Glanzmann-Naegeli disorder
  • Platelet production finding
  • thromboasthenia
  • Platelet storage organelle defect
  • PLATELET FIBRINOGEN RECEPTOR DEFICIENCY
  • Acquired PF-3 disease
  • Hereditary platelet function disorder
  • Congenital dyserythropoietic anemia
  • Deficiency of glycoprotein complex IIb-IIIa
  • CDA - congenital dyserythropoietic anaemia
  • Congenital miosis
  • BLEEDING DISORDER, PLATELET-TYPE, 4
  • Acquired thrombocytopathy
  • Hereditary platelet disorder
  • Delta storage pool disease
  • Storage pool deficiency
  • Stormorken-Sjaastad-Langslet syndrome
  • X-linked dyserythropoietic anaemia with abnormal platelets and neutropenia
  • Qualitative platelet disorder
  • GP IIb-IIIa Complex, Deficiency Of
  • Thromboxane generation defect
  • White platelet syndrome
  • Gray platelet syndrome (disorder)
  • Secretion defect of platelets
  • Sensitised cell
  • Thrombasthenias
  • thrombocytasthenia
  • Constricted pupil
  • GPS
  • Familial alpha>2< adrenergic receptor defect in platelets
  • Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type
Frequently Asked Questions
What is the ICD-10 code for qualitative platelet defects?

The ICD-10-CM code for qualitative platelet defects is D69.1. The full clinical description is "Qualitative platelet defects". D69.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D69.1 mean?

ICD-10-CM code D69.1 represents “Qualitative platelet defects”. 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 D69.1 a billable code?

Yes, D69.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D69.1 in?

D69.1 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D69.1?

D69.1 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 5 more.

What SNOMED CT codes does D69.1 map to?

D69.1 maps to 62 SNOMED CT concepts: 75542001, 112141008, 129654004, 234479004, 128095007, and 57 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D69.1?

D69.1 is linked to 5 UMLS Concept Unique Identifiers: C0040015, C0272302, C2873804, C0235604, C2873805. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D69.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like qualitative platelet defects 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 D69.1?

D69.1 maps to the ICD-11 code: 3B62.Z (Qualitative platelet defects, unspecified).

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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.