P53
BillableHemorrhagic disease of newborn
Hemorrhagic disease of newborn
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Vitamin K deficiency of newborn
Includes
Conditions included under this code
- 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
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
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(127)
SNOMED CT
- Bleeding diathesis due to vitamin K deficiency1286003
- Vitamin K deficiency coagulation disorder1286003
- HDN - Haemorrhagic disease of newborn12546009
- HDN - Hemorrhagic disease of newborn12546009
- Haemorrhagic diathesis of newborn12546009
- Haemorrhagic disease of the newborn12546009
- Haemorrhagic disease of the newborn due to vitamin K deficiency12546009
- Hemorrhagic diathesis of newborn12546009
- Hemorrhagic disease of the newborn12546009
- Hemorrhagic disease of the newborn due to vitamin K deficiency12546009
- Neonatal vitamin K deficiency12546009
- Vitamin K deficiency of newborn12546009
- Vitamin K deficiency of the newborn12546009
- Acquired neonatal factor II deficiency disease24149006
- Haemorrhagic disease of the newborn due to factor II deficiency24149006
- Hemorrhagic disease of the newborn due to factor II deficiency24149006
- Abnormal fibrinolysis30257002
- Deficiency of vitamin K52675005
- Vitamin K deficiency52675005
- Decreased fibrinolysis87066005
- Neonatal coagulation disorder95623001
- Deficiency of coagulation factor due to vitamin K deficiency191297009
- Fibrinolytic bleeding syndrome234464006
- Alpha-2-antiplasmin deficiency234465007
- Deficiency of vitamin K1386073005
- Disorder of vitamin K386074004
- Disorder of vitamin K1386075003
- Disorder of vitamin K>1<386075003
- Disorder of vitamin K2386076002
- Disorder of vitamin K>2<386076002
- Deficiency of vitamin K2386077006
- Deficiency of vitamin K>2<386077006
- Hereditary combined coagulation factor deficiency439157002
- Congenital alpha-2-antiplasmin deficiency716746003
- Congenital alpha2-antiplasmin deficiency716746003
- Early onset diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of foetus and newborn717935003
- Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn717935003
- Classic onset haemorrhagic disease of newborn due to vitamin K deficiency717936002
- Classic onset hemorrhagic disease of newborn due to vitamin K deficiency717936002
- Late onset diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of fetus and newborn717937006
- Late onset diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of foetus and newborn717937006
- Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn717937006
- Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency717941005
- PXE (pseudoxanthoma elasticum) like syndrome717941005
- Pseudoxanthoma elasticum-like syndrome717941005
- Hereditary combined deficiency of factors II, VII, IX and X724356003
- Hereditary combined deficiency of vitamin K-dependent clotting factors724356003
UMLS
- HDN - Haemorrhagic disease of newbornC0019088
- HDN - Hemorrhagic disease of newbornC0019088
- HEMORRHAGIC DIS NEWBORNC0019088
- Haemorrhagic diathesis of newbornC0019088
- Haemorrhagic disease of newbornC0019088
- Haemorrhagic disease of the newbornC0019088
- Haemorrhagic disease of the newborn due to vitamin K deficiencyC0019088
- Hemorrhagic Disease of NewbornC0019088
- Hemorrhagic diathesis of newbornC0019088
- Hemorrhagic disease of newbornC0019088
- Hemorrhagic disease of the newbornC0019088
- Hemorrhagic disease of the newborn due to vitamin K deficiencyC0019088
- Hemorrhagic disease of the newborn due to vitamin K deficiency (disorder)C0019088
- Neonatal vitamin K deficiencyC0019088
- Newborn Hemorrhagic DiseaseC0019088
- Newborn Hemorrhagic DiseasesC0019088
- Vitamin K Deficiency Bleeding in NewbornC0019088
- Vitamin K deficiency of newbornC0019088
- Vitamin K deficiency of the newbornC0019088
- disease haemorrhagic newbornC0019088
- disease hemorrhagic newbornC0019088
- hemorrhagic disease newbornC0019088
- hemorrhagic disease of newbornC0019088
- newborn hemorrhagic diseaseC0019088
Clinical Terms
- Vitamin K Deficiency Bleeding in Newborn
- Body skin hyperlaxity due to vitamin K dependent coagulation factor deficiency
- Acquired neonatal factor II deficiency disease
- Haemorrhagic disease of the newborn due to factor II deficiency
- Neonatal vitamin K deficiency
- HDN - Hemorrhagic disease of newborn
- Disorder of vitamin K>1<
- newborn hemorrhagic disease
- Newborn Hemorrhagic Diseases
- Hemorrhagic disease of the newborn
- Neonatal coagulation disorder
- Hereditary combined coagulation factor deficiency
- Early onset diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of foetus and newborn
- Deficiency of vitamin K2
- Decreased fibrinolysis
- Haemorrhagic diathesis of newborn
- Late onset diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of fetus and newborn
- Alpha-2-antiplasmin deficiency
- disease hemorrhagic newborn
- Congenital alpha2-antiplasmin deficiency
- Disorder of vitamin K1
- Congenital alpha-2-antiplasmin deficiency
- Classic onset haemorrhagic disease of newborn due to vitamin K deficiency
- Vitamin K deficiency of the newborn
- Hemorrhagic disease of the newborn due to vitamin K deficiency
- Hemorrhagic disease of the newborn due to vitamin K deficiency (disorder)
- Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn
- HDN - Haemorrhagic disease of newborn
- Disorder of vitamin K>2<
- Bleeding diathesis due to vitamin K deficiency
- Hereditary combined deficiency of vitamin K-dependent clotting factors
- Vitamin K deficiency
- Vitamin K deficiency coagulation disorder
- Abnormal fibrinolysis
- HEMORRHAGIC DIS NEWBORN
- disease haemorrhagic newborn
- Hemorrhagic diathesis of newborn
- Disorder of vitamin K2
- Late onset diffuse bleeding diathesis secondary to vitamin K deficient haemorrhagic disease of foetus and newborn
- Hereditary combined deficiency of factors II, VII, IX and X
- Haemorrhagic disease of newborn
- Deficiency of vitamin K
- Pseudoxanthoma elasticum-like syndrome
- Fibrinolytic bleeding syndrome
- Hemorrhagic disease of the newborn due to factor II deficiency
- Classic onset hemorrhagic disease of newborn due to vitamin K deficiency
- hemorrhagic disease newborn
- Disorder of vitamin K
- Deficiency of vitamin K1
- PXE (pseudoxanthoma elasticum) like syndrome
- Haemorrhagic disease of the newborn due to vitamin K deficiency
- Vitamin K deficiency of newborn
- Deficiency of coagulation factor due to vitamin K deficiency
- Deficiency of vitamin K>2<
- Haemorrhagic disease of the newborn
- Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn
Frequently Asked Questions
What is the ICD-10 code for hemorrhagic disease of newborn?
The ICD-10-CM code for hemorrhagic disease of newborn is P53. The full clinical description is "Hemorrhagic disease of newborn". P53 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code P53 mean?
ICD-10-CM code P53 represents “Hemorrhagic disease of newborn”. It is classified under Chapter 16: Certain Conditions Originating in the Perinatal Period and is a billable/specific code that can be used on a claim.
Is P53 a billable code?
Yes, P53 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is P53 in?
P53 is in Chapter 16: Certain Conditions Originating in the Perinatal Period (codes P00-P96).
What codes cannot be used with P53?
P53 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital stenosis and stricture of bile ducts (Q44.3); Crigler-Najjar syndrome (E80.5); Dubin-Johnson syndrome (E80.6); and 2 more.
What SNOMED CT codes does P53 map to?
P53 maps to 22 SNOMED CT concepts: 30257002, 24149006, 234465007, 1286003, 717941005, and 17 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for P53?
P53 is linked to 1 UMLS Concept Unique Identifier: C0019088. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does P53 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hemorrhagic disease of newborn 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 P53?
P53 maps to the ICD-11 code: KA8F.0 (Diffuse bleeding diathesis due to vitamin K deficient haemorrhagic disease of fetus or newborn).
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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.