DRG 813

Medical DRG

Coagulation Disorders

TypeMedicalMDC16Dx Codes39

What is MS-DRG 813?

MS-DRG 813 is a Medical Medicare Severity Diagnosis Related Group under Major Diagnostic Category 16 (MDC 16). It maps to 39 ICD-10-CM diagnosis codes. For FY 2026 it carries a relative weight of 1.5253 with a geometric mean length of stay of 3.6 days and an arithmetic mean of 4.7 days. Hospitals use this grouping to determine reimbursement for inpatient stays under Medicare.

Classification
Medical DRG
Diagnosis-driven grouping
Linked Codes
39 diagnosis
Billable Dx
100%
39 of 39 shown

FY 2026 Payment Data

Official values from Table 5 of the FY 2026 IPPS Final Rule (CMS).

Relative Weight
1.5253
Payment multiplier vs. average case (1.0)
Geometric Mean LOS
3.6 days
Used for transfer payment calculations
Arithmetic Mean LOS
4.7 days
Average length of stay
Post-Acute Transfer
No
Not subject to the transfer policy

Linked ICD-10-CM Diagnosis Mappings

  • D65

    Disseminated intravascular coagulation [defibrination syndrome]

    BillableChapter 3
  • D66

    Hereditary factor VIII deficiency

    BillableChapter 3
  • D67

    Hereditary factor IX deficiency

    BillableChapter 3
  • D68.00

    Von Willebrand disease, unspecified

    BillableChapter 3
  • D68.01

    Von Willebrand disease, type 1

    BillableChapter 3
  • D68.020

    Von Willebrand disease, type 2A

    BillableChapter 3
  • D68.021

    Von Willebrand disease, type 2B

    BillableChapter 3
  • D68.022

    Von Willebrand disease, type 2M

    BillableChapter 3
  • D68.023

    Von Willebrand disease, type 2N

    BillableChapter 3
  • D68.029

    Von Willebrand disease, type 2, unspecified

    BillableChapter 3
  • D68.03

    Von Willebrand disease, type 3

    BillableChapter 3
  • D68.04

    Acquired von Willebrand disease

    BillableChapter 3
  • D68.09

    Other von Willebrand disease

    BillableChapter 3
  • D68.1

    Hereditary factor XI deficiency

    BillableChapter 3
  • D68.2

    Hereditary deficiency of other clotting factors

    BillableChapter 3
  • D68.311

    Acquired hemophilia

    BillableChapter 3
  • D68.318

    Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors

    BillableChapter 3
  • D68.32

    Hemorrhagic disorder due to extrinsic circulating anticoagulants

    BillableChapter 3
  • D68.4

    Acquired coagulation factor deficiency

    BillableChapter 3
  • D68.8

    Other specified coagulation defects

    BillableChapter 3
  • D68.9

    Coagulation defect, unspecified

    BillableChapter 3
  • D69.0

    Allergic purpura

    BillableChapter 3
  • D69.1

    Qualitative platelet defects

    BillableChapter 3
  • D69.2

    Other nonthrombocytopenic purpura

    BillableChapter 3
  • D69.3

    Immune thrombocytopenic purpura

    BillableChapter 3
  • D69.41

    Evans syndrome

    BillableChapter 3
  • D69.42

    Congenital and hereditary thrombocytopenia purpura

    BillableChapter 3
  • D69.49

    Other primary thrombocytopenia

    BillableChapter 3
  • D69.51

    Posttransfusion purpura

    BillableChapter 3
  • D69.59

    Other secondary thrombocytopenia

    BillableChapter 3
  • D69.6

    Thrombocytopenia, unspecified

    BillableChapter 3
  • D69.8

    Other specified hemorrhagic conditions

    BillableChapter 3
  • D69.9

    Hemorrhagic condition, unspecified

    BillableChapter 3
  • D75.821

    Non-immune heparin-induced thrombocytopenia

    BillableChapter 3
  • D75.822

    Immune-mediated heparin-induced thrombocytopenia

    BillableChapter 3
  • D75.828

    Other heparin-induced thrombocytopenia syndrome

    BillableChapter 3
  • D75.829

    Heparin-induced thrombocytopenia, unspecified

    BillableChapter 3
  • D75.84

    Other platelet-activating anti-PF4 disorders

    BillableChapter 3
  • R23.3

    Spontaneous ecchymoses

    BillableChapter 18