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) 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)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code D69.8?
ICD-10-CM code D69.8 represents "Other specified hemorrhagic conditions". It 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.
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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.