-
ICD-10-CM Codes
›
-
P00-P96
Certain conditions originating in the perinatal period
›
-
P50-P61
Hemorrhagic and hematological disorders of newborn
›
-
P61-
Other perinatal hematological disorders
›
-
2021 ICD-10-CM Diagnosis Code P61.6
2021 ICD-10-CM Diagnosis Code P61.6
Other transient neonatal disorders of coagulation
2016 2017 2018 2019 2020 2021 Billable/Specific Code Code on Newborn Record
- P61.6 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2021 edition of ICD-10-CM P61.6 became effective on October 1, 2020.
- This is the American ICD-10-CM version of P61.6 - other international versions of ICD-10 P61.6 may differ.
ICD-10-CM Coding Rules
- P61.6 should be used on the newborn record - not on the maternal record.
The following code(s) above
P61.6 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
P61.6:
- P00-P96
2021 ICD-10-CM Range P00-P96
Certain conditions originating in the perinatal periodIncludes- conditions that have their origin in the fetal or perinatal period (before birth through the first 28 days after birth) even if morbidity occurs later
Note- Codes from this chapter are for use on newborn records only, never on maternal records
Type 2 Excludes- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- tetanus neonatorum (A33)
Certain conditions originating in the perinatal period - P50-P61
2021 ICD-10-CM Range P50-P61
Hemorrhagic and hematological disorders of newbornType 1 Excludes- congenital stenosis and stricture of bile ducts (Q44.3)
- Crigler-Najjar syndrome (E80.5)
- Dubin-Johnson syndrome (E80.6)
- Gilbert syndrome (E80.4)
- hereditary hemolytic anemias (D55-D58)
Hemorrhagic and hematological disorders of newborn - P61
ICD-10-CM Diagnosis Code P61
Other perinatal hematological disorders
2016 2017 2018 2019 2020 2021 Non-Billable/Non-Specific Code
Type 1 Excludes- transient hypogammaglobulinemia of infancy (D80.7)
Other perinatal hematological disorders
Approximate Synonyms
- Neonatal coagulation disorder
ICD-10-CM P61.6 is grouped within Diagnostic Related Group(s) (MS-DRG v38.0):
- 791 Prematurity with major problems
- 793 Full term neonate with major problems
Convert P61.6 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- Abnormal, abnormality, abnormalities - see also Anomaly
- coagulation D68.9
ICD-10-CM Diagnosis Code D68.9
Coagulation defect, unspecified
2016 2017 2018 2019 2020 2021 Billable/Specific Code
- Defect, defective Q89.9
ICD-10-CM Diagnosis Code Q89.9
Congenital malformation, unspecified
2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Applicable To- Congenital anomaly NOS
- Congenital deformity NOS
- Deficiency, deficient
- coagulation NOS D68.9
ICD-10-CM Diagnosis Code D68.9
Coagulation defect, unspecified
2016 2017 2018 2019 2020 2021 Billable/Specific Code
- Disorder (of) - see also Disease
- Hypoprothrombinemia (congenital) (hereditary) (idiopathic) D68.2
ICD-10-CM Diagnosis Code D68.2
Hereditary deficiency of other clotting factors
2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To- AC globulin deficiency
- Congenital afibrinogenemia
- Deficiency of factor I [fibrinogen]
- Deficiency of factor II [prothrombin]
- Deficiency of factor V [labile]
- Deficiency of factor VII [stable]
- Deficiency of factor X [Stuart-Prower]
- Deficiency of factor XII [Hageman]
- Deficiency of factor XIII [fibrin stabilizing]
- Dysfibrinogenemia (congenital)
- Hypoproconvertinemia
- Owren's disease
- Proaccelerin deficiency
ICD-10-CM Codes Adjacent To P61.6
P59.8 Neonatal jaundice from other specified causes
P59.9 Neonatal jaundice, unspecified
P60 Disseminated intravascular coagulation of newborn
P61 Other perinatal hematological disorders
P61.0 Transient neonatal thrombocytopenia
P61.1 Polycythemia neonatorum
P61.2 Anemia of prematurity
P61.3 Congenital anemia from fetal blood loss
P61.4 Other congenital anemias, not elsewhere classified
P61.5 Transient neonatal neutropenia
P61.6
Other transient neonatal disorders of coagulation
P61.8 Other specified perinatal hematological disorders
P61.9 Perinatal hematological disorder, unspecified
P70 Transitory disorders of carbohydrate metabolism specific to newborn
P70.0 Syndrome of infant of mother with gestational diabetes
P70.1 Syndrome of infant of a diabetic mother
P70.2 Neonatal diabetes mellitus
P70.3 Iatrogenic neonatal hypoglycemia
P70.4 Other neonatal hypoglycemia
P70.8 Other transitory disorders of carbohydrate metabolism of newborn
P70.9 Transitory disorder of carbohydrate metabolism of newborn, unspecified
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.