P78.89
BillableOther specified perinatal digestive system disorders
Other specified perinatal digestive system disorders
Coding Notes
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)
- cystic fibrosis (E84.0-E84.9)
- neonatal gastrointestinal hemorrhages (P54.0-P54.3)
Excludes 2
Conditions not included here, but the patient may have both
Also Known As / Clinical Terms
SNOMED CT
- Dermatitis of the newborn7392002
- Inflammatory dermatosis of newborn7392002
- Neonatal dermatitis7392002
- PP - Pneumoperitoneum17204006
- Peritoneal cavity free air17204006
- Pneumoperitoneum17204006
- Familial intrahepatic cholestasis74162007
- Fatal intrahepatic cholestasis74162007
- PFIC - progressive familial intrahepatic cholestasis74162007
- Progressive familial intrahepatic cholestasis74162007
- Progressive intrahepatic cholestasis74162007
- Neonatal hepatocellular damage95555006
- Haemophagocytic lymphohistiocytosis234437005
- Haemophagocytic syndrome234437005
- Hemophagocytic lymphohistiocytosis234437005
- Hemophagocytic syndrome234437005
- Hyperinflammatory lymphohistiocytosis234437005
- Sclerosing cholangitis235917005
- Gastrointestinal hormone-secreting endocrine tumor237832001
- Gastrointestinal hormone-secreting endocrine tumour237832001
- Transient neonatal colitis276523005
- Gastritis of newborn276527006
- Perinatal pneumoperitoneum277636009
- Hepatocellular liver damage419616000
- Haemophagocytic lymphohistiocytosis with rheumatologic disease430478003
- Hemophagocytic lymphohistiocytosis with rheumatologic disease430478003
- Macrophage activation syndrome430478003
- Reactive haemophagocytic syndrome430478003
- Reactive hemophagocytic syndrome430478003
- Cholestasis in newborn433237003
- Neonatal cholestasis433237003
- Esophagitis in newborn721611000
- Neonatal esophagitis721611000
- Neonatal oesophagitis721611000
- Neonatal malabsorption co-occurrent and due to gastrointestinal hormone-secreting endocrine tumor735718000
- Neonatal malabsorption co-occurrent and due to gastrointestinal hormone-secreting endocrine tumour735718000
- Neonatal malabsorption with gastrointestinal hormone-secreting endocrine tumor735718000
- Neonatal malabsorption with gastrointestinal hormone-secreting endocrine tumour735718000
- Disorder of oral mucosa in neonate737211006
- Neonatal disorder of oral mucosa737211006
- Neonatal inflammatory skin and bowel disease773662009
- BSEP (bile salt export pump) deficiency1155841005
- PFIC2 - progressive familial intrahepatic cholestasis type 21155841005
- Progressive familial intrahepatic cholestasis type 21155841005
- NLRC4-related autoinflammatory syndrome with macrophage activation syndrome1197594000
- NLRC4-related infantile enterocolitis, autoinflammatory syndrome1197594000
- NLRC4-related macrophage activation syndrome1197594000
- Periodic fever, infantile enterocolitis, autoinflammatory syndrome1197594000
- Isolated neonatal sclerosing cholangitis1220580006
Frequently Asked Questions
What is the ICD-10 code for other specified perinatal digestive system disorders?
The ICD-10-CM code for other specified perinatal digestive system disorders is P78.89. The full clinical description is "Other specified perinatal digestive system disorders". P78.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code P78.89 mean?
ICD-10-CM code P78.89 represents "Other specified perinatal digestive system disorders". 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 P78.89 a billable code?
Yes, P78.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is P78.89 in?
P78.89 is in Chapter 16: Certain Conditions Originating in the Perinatal Period (codes P00-P96).
What codes cannot be used with P78.89?
P78.89 has Excludes1 notes indicating codes that cannot be used together with it, including: cystic fibrosis (E84.0-E84.9); neonatal gastrointestinal hemorrhages (P54.0-P54.3).
What SNOMED CT codes does P78.89 map to?
P78.89 maps to 20 SNOMED CT concepts: 1155841005, 433237003, 7392002, 737211006, 721611000, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for P78.89?
P78.89 is linked to 1 UMLS Concept Unique Identifier: C0159007. 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.