D69.8
BillableOther specified hemorrhagic conditions
Other specified hemorrhagic conditions
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Capillary fragility (hereditary)
- Vascular pseudohemophilia
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
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(8)
D69.0Allergic purpura
D69.1Qualitative platelet defects
D69.2Other nonthrombocytopenic purpura
D69.3Immune thrombocytopenic purpura
D69.4Other primary thrombocytopenia
D69.5Secondary thrombocytopenia
D69.6Thrombocytopenia, unspecified
D69.9Hemorrhagic condition, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(141)
SNOMED CT
- Vascular haemostatic disease21112004
- Vascular hemostatic disease21112004
- Vascular purpura21112004
- Decreased platelet production25533006
- Capillary haemorrhage43696002
- Capillary hemorrhage43696002
- Increased capillary fragility56888007
- Capillary fragility abnormality91304009
- Secondary thrombocytopenia154826009
- Secondary non-thrombocytopenic purpura234495004
- Fragile blood vessel248708004
- Friable blood vessel248708004
- Fragile capillaries248726001
- Capillary fragillity - finding366213003
- Finding of capillary fragillity366213003
- Platelet production finding415117004
- Pseudothrombocytopenia721119004
- Purpura of skin co-occurrent and due to vascular fragility737243006
- Bleeding diathesis due to thromboxane synthesis deficiency783194008
- Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder1172901009
- PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction1172901009
- PLA2G4A-related platelet dysfunction1172901009
- Platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency1172901009
UMLS
- AngiohaemophiliaC0042974
- AngiohemophiliaC0042974
- AngiohemophiliasC0042974
- Constitutional thrombopathyC0042974
- Disorder, Von WillebrandC0042974
- Factor VIII Rag deficiencyC0042974
- Factor VIII deficiency with vascular defectC0042974
- Hemophilia, VascularC0042974
- PseudohaemophiliaC0042974
- Pseudohaemophilia type BC0042974
- PseudohemophiliaC0042974
- Pseudohemophilia type BC0042974
- Pseudohemophilia, VascularC0042974
- Pseudohemophilias, VascularC0042974
- VON WILLEBRAND DISC0042974
- VON WILLEBRANDS DISC0042974
- Vascular HemophiliaC0042974
- Vascular HemophiliasC0042974
- Vascular PseudohemophiliaC0042974
- Vascular PseudohemophiliasC0042974
- Vascular haemophiliaC0042974
- Vascular hemophiliaC0042974
- Vascular pseudohemophiliaC0042974
- Von Willebrand DisorderC0042974
- Von Willebrand diseaseC0042974
- Von Willebrand disease, unspecifiedC0042974
- Von Willebrand disorderC0042974
- Von Willebrand's Factor DeficiencyC0042974
- Von Willebrand's diseaseC0042974
- Von Willebrand's factor deficiencyC0042974
- angiohemophiliaC0042974
- disease von willebrandC0042974
- disease von willebrandsC0042974
- diseases von willebrand'sC0042974
- pseudohemophiliaC0042974
- vWD - von Willebrand's diseaseC0042974
- vascular hemophiliaC0042974
- von Willebrand DiseaseC0042974
- von Willebrand DiseasesC0042974
- von Willebrand diseaseC0042974
- von Willebrand disorderC0042974
- von Willebrand disorder (disorder)C0042974
- von Willebrand's DiseaseC0042974
- von Willebrand's DiseasesC0042974
- von Willebrand's diseaseC0042974
- von Willebrand-Jurgens diseaseC0042974
- von willebrand diseaseC0042974
- von willebrand disorderC0042974
- von willebrand's diseaseC0042974
- von willebrands diseaseC0042974
- Capillary fragility (hereditary)C0340804
- Capillary fragility - hereditaryC0340804
- Hereditary vascular fragilityC0340804
- Hereditary vascular fragility (disorder)C0340804
- Other Specified Hemorrhagic ConditionsC0029804
- Other specified hemorrhagic conditionsC0029804
Clinical Terms
- Angiohemophilias
- Angiohemophilia
- Pseudothrombocytopenia
- Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
- Secondary thrombocytopenia
- Factor VIII Rag deficiency
- Capillary fragility - hereditary
- Finding of capillary fragillity
- Pseudohemophilia, Vascular
- VON WILLEBRAND DIS
- diseases von willebrand's
- von willebrands disease
- Capillary fragillity - finding
- Von Willebrand disorder
- von Willebrand-Jurgens disease
- Vascular pseudohemophilia
- PLA2G4A-related platelet dysfunction
- VON WILLEBRANDS DIS
- vWD - von Willebrand's disease
- Pseudohaemophilia type B
- Vascular Pseudohemophilias
- Pseudohemophilias, Vascular
- Vascular purpura
- Capillary fragility abnormality
- Vascular Hemophilias
- von willebrand disease
- Platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency
- von Willebrand Diseases
- Von Willebrand disease, unspecified
- Angiohaemophilia
- Von Willebrand's disease
- Pseudohemophilia type B
- pseudohemophilia
- Constitutional thrombopathy
- Factor VIII deficiency with vascular defect
- Vascular hemophilia
- Secondary non-thrombocytopenic purpura
- Hemophilia, Vascular
- Bleeding diathesis due to thromboxane synthesis deficiency
- Friable blood vessel
- Disorder, Von Willebrand
- Vascular haemophilia
- von Willebrand's Diseases
- Decreased platelet production
- Pseudohaemophilia
- Purpura of skin co-occurrent and due to vascular fragility
- Von Willebrand's factor deficiency
- Capillary haemorrhage
- Increased capillary fragility
- Platelet production finding
- Fragile blood vessel
- Capillary fragility (hereditary)
- PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction
- Hereditary vascular fragility
- Vascular hemostatic disease
- disease von willebrands
- Fragile capillaries
- von Willebrand disorder (disorder)
- disease von willebrand
- Hereditary vascular fragility (disorder)
- Vascular haemostatic disease
- Capillary hemorrhage
Frequently Asked Questions
What is the ICD-10 code for other specified hemorrhagic conditions?
The ICD-10-CM code for other specified hemorrhagic conditions is D69.8. The full clinical description is "Other specified hemorrhagic conditions". D69.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D69.8 mean?
ICD-10-CM code D69.8 represents “Other specified hemorrhagic conditions”. 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 D69.8 a billable code?
Yes, D69.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D69.8 in?
D69.8 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D69.8?
D69.8 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 4 more.
What SNOMED CT codes does D69.8 map to?
D69.8 maps to 15 SNOMED CT concepts: 783194008, 91304009, 366213003, 43696002, 1172901009, and 10 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D69.8?
D69.8 is linked to 3 UMLS Concept Unique Identifiers: C0042974, C0340804, C0029804. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D69.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified hemorrhagic conditions 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 D69.8?
D69.8 maps to the ICD-11 code: 3B4Z (Coagulation 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.