D69.1
BillableQualitative platelet defects
Qualitative platelet defects
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)
- benign hypergammaglobulinemic purpura (D89.0)
- cryoglobulinemic purpura (D89.1)
- essential (hemorrhagic) thrombocythemia (D47.3)
- hemorrhagic thrombocythemia (D47.3)
- purpura fulminans (D65)
- thrombotic thrombocytopenic purpura (M31.19)
- Waldenström hypergammaglobulinemic purpura (D89.0)
- hemolytic-uremic syndrome (D59.3-)
Excludes 2
Conditions not included here, but the patient may have both
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- von Willebrand disease (D68.0-)
Also Known As / Clinical Terms
SNOMED CT
- Autoimmune state4301008
- Autoimmunity4301008
- Delta storage pool disease9417000
- Dense body deficiency9417000
- Nucleotide storage pool disorder9417000
- Platelet dense granule deficiency9417000
- Platelet dysfunction caused by aspirin17592003
- Platelet disorder22716005
- Thrombocytopathy22716005
- Glanzmann thromboasthenia32942005
- Glanzmann's disease32942005
- Glanzmann's syndrome32942005
- Glanzmann's thrombasthenia32942005
- Glanzmann-Naegeli disorder32942005
- Hereditary haemorrhagic thrombasthenia32942005
- Hereditary hemorrhagic thrombasthenia32942005
- Hereditary thromboasthenia32942005
- Thrombasthenia32942005
- Platelet procoagulant activity deficiency43346008
- Platelet secretory disorder51448009
- Secretion defect of platelets51448009
- Deficient alpha granule syndrome51720005
- Gray platelet syndrome51720005
- Grey platelet syndrome51720005
- Platelet alpha granule deficiency51720005
- Platelet granule defect51720005
- CDA - congenital dyserythropoietic anaemia52951008
- CDA - congenital dyserythropoietic anemia52951008
- Congenital dyserythropoietic anaemia52951008
- Congenital dyserythropoietic anemia52951008
- Sensitised cell52976009
- Sensitized cell52976009
- Bernard Soulier syndrome54569005
- Bernard-Soulier syndrome54569005
- Mediterranean macrothrombocytopenia60628003
- Increased platelet destruction62781006
- Autosensitivity62978008
- Sensitised platelet65533007
- Sensitized platelet65533007
- Decreased platelet destruction68318002
- Abnormal platelet destruction75542001
- Decreased platelet life span75944007
- Autoplatelet sensitivity81535001
- Ineffective thrombopoiesis91504005
- Abnormal platelet production112141008
- Acquired platelet function disorder128095007
- Acquired thrombocytopathy128095007
- Hereditary platelet function disorder128096008
- Scott syndrome128098009
- Platelet storage organelle defect128099001
- Platelet storage pool defect128099001
- Mixed alpha granule and dense body deficiency128100009
- Familial alpha>2< adrenergic receptor defect in platelets128102001
- Isolated collagen aggregation defect128103006
- Acquired PF-3 disease129654004
- Acquired platelet factor 3 disease129654004
- Platelet clumps134204007
- Hereditary platelet disorder234469001
- Hereditary thrombocytopathy234469001
- Inherited platelet disorder234469001
- Platelet membrane defect234470000
- Glycoprotein Ia defect234471001
- Glycoprotein Ib defect234472008
- Dense body defect234474009
- Storage pool deficiency234474009
- Thromboxane generation defect234475005
- Cyclooxygenase deficiency234476006
- Thromboxane synthetase deficiency234477002
- Giant platelet syndrome234478007
- Acquired platelet disorder234479004
- Megakaryocytic thrombocytopenia234483004
- Montreal platelet syndrome234486007
- Montreal syndrome234486007
- Qualitative platelet defect267532001
- Qualitative platelet disorder267532001
- Acquired storage pool deficiency (platelets)296332004
- Exhausted platelets297307009
- Constricted pupil301939004
- Miosis301939004
- Miotic pupil301939004
- Pupil constriction301939004
- Small pupil301939004
- Platelet sequestration322096003
- Finding of platelet morphology365633003
- Platelet morphology - finding365633003
- Congenital miosis400962005
- Megakaryocyte finding414660003
- Platelet production finding415117004
- Platelet dysfunction associated with uraemia421132004
- Platelet dysfunction associated with uremia421132004
- Uraemic platelet dysfunction421132004
- Uremic platelet dysfunction421132004
- Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type441134009
- Asplenia707147002
- Stormorken syndrome711407000
- Stormorken-Sjaastad-Langslet syndrome711407000
- Thrombocytopathy, asplenia and miosis711407000
- White platelet syndrome718553004
- Medich giant platelet syndrome718554005
- Medich macrothrombocytopenia718554005
- Familial platelet disorder with associated myeloid malignancy725034002
- Familial platelet syndrome with predisposition to acute myelogenous leukaemia725034002
- Familial platelet syndrome with predisposition to acute myelogenous leukemia725034002
- Bleeding disorder due to glycoprotein VI deficiency765977002
- Bleeding disorder platelet-type 11765977002
- Glycoprotein VI deficiency765977002
- X-linked dyserythropoietic anaemia with abnormal platelets and neutropenia782759001
- X-linked dyserythropoietic anemia with abnormal platelets and neutropenia782759001
- Bleeding diathesis due to collagen receptor defect782934004
- Platelet satellite1156624002
- Platelet satellitism1156624002
UMLS
- BDPLT2C0040015
- BLEEDING DISORDER, PLATELET-TYPE, 2C0040015
- Deficiency of GP 2b 3a ComplexC0040015
- Deficiency of glycoprotein complex IIb-IIIaC0040015
- Deficiency of platelet fibrinogen receptorC0040015
- GLANZMANN THROMBASTHENIAC0040015
- GLANZMANN THROMBASTHENIA 1C0040015
- GLYCOPROTEIN COMPLEX IIb-IIIa DEFICIENCYC0040015
- GP IIb IIIa Complex, Deficiency OfC0040015
- GP IIb-IIIa COMPLEX DEFICIENCYC0040015
- GP IIb-IIIa Complex, Deficiency OfC0040015
- GT1C0040015
- Glanzmann ThrombastheniaC0040015
- Glanzmann Thrombasthenia, Type AC0040015
- Glanzmann diseaseC0040015
- Glanzmann thrombastheniaC0040015
- Glanzmann thromboastheniaC0040015
- Glanzmann's diseaseC0040015
- Glanzmann's syndromeC0040015
- Glanzmann's thrombastheniaC0040015
- Glanzmann's thrombasthenia (disorder)C0040015
- Glanzmann-Naegeli disorderC0040015
- Glycoprotein Complex IIb IIIa, Deficiency OfC0040015
- Glycoprotein Complex IIb-IIIa, Deficiency OfC0040015
- Glycoprotein IIb/IIIa defectC0040015
- Hereditary haemorrhagic thrombastheniaC0040015
- Hereditary hemorrhagic thrombastheniaC0040015
- Hereditary thrombastheniaC0040015
- Hereditary thromboastheniaC0040015
- PLATELET FIBRINOGEN RECEPTOR DEFICIENCYC0040015
- PLATELET GLYCOPROTEIN IIb-IIIa DEFICIENCYC0040015
- Platelet Fibrinogen Receptor, Deficiency ofC0040015
- Platelet Glycoprotein 2b 3a DeficiencyC0040015
- Platelet Glycoprotein 2b-3a DeficiencyC0040015
- Platelet Glycoprotein IIb IIIa DeficiencyC0040015
- Platelet Glycoprotein IIb-IIIa DeficiencyC0040015
- Platelet fibrinogen receptor deficiencyC0040015
- THROMBASTHENIA OF GLANZMANN AND NAEGELIC0040015
- ThrombastheniaC0040015
- Thrombasthenia of Glanzmann and NaegeliC0040015
- Thrombasthenia, GlanzmannC0040015
- ThrombastheniasC0040015
- ThromboastheniaC0040015
- glanzmann thrombastheniaC0040015
- glanzmann's diseaseC0040015
- glanzmann's thrombastheniaC0040015
- glanzmanns thrombastheniaC0040015
- thrombastheniaC0040015
- thromboastheniaC0040015
- thrombocytastheniaC0040015
- BDPLT4C0272302
- BLEEDING DISORDER, PLATELET-TYPE, 4C0272302
- Bleeding disorder, platelet-type, 4C0272302
- Deficient alpha granule syndromeC0272302
- GPSC0272302
- GRAY PLATELET SYNDROMEC0272302
- Gray Platelet SyndromeC0272302
- Gray Platelet SyndromesC0272302
- Gray platelet syndromeC0272302
- Gray platelet syndrome (disorder)C0272302
- Grey Platelet SyndromeC0272302
- Grey Platelet SyndromesC0272302
- Grey platelet syndromeC0272302
- PLATELET ALPHA-GRANULE DEFICIENCYC0272302
- Platelet Syndromes, GreyC0272302
- Platelet alpha granule deficiencyC0272302
- Platelet granule defectC0272302
- Syndrome, Gray PlateletC0272302
- Syndrome, Grey PlateletC0272302
- Syndromes, Gray PlateletC0272302
- gray platelet syndromeC0272302
- grey platelet syndromeC0272302
- Bernard-Soulier [giant platelet] syndromeC2873804
- Qualitative platelet defectC0235604
- Qualitative platelet defectsC0235604
- ThrombocytopathyC0235604
- Thromboasthenia (hemorrhagic) (hereditary)C2873805
Frequently Asked Questions
What is ICD-10 code D69.1?
ICD-10-CM code D69.1 represents "Qualitative platelet defects". It 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.
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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.