P53
BillableHemorrhagic disease of newborn
Hemorrhagic disease of newborn
Status
Billable / Specific
Block
P50-P61
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
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code P53?
ICD-10-CM code P53 represents "Hemorrhagic disease of newborn". It 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: 12546009, 30257002, 24149006, 234465007, 1286003, 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.
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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.