AutoICD API

P78.89

Billable

Other specified perinatal digestive system disorders

Other specified perinatal digestive system disorders

Status

Billable / Specific

Block

P76-P78

Parent Code

P78.8

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)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(4)
P78.81

Congenital cirrhosis (of liver)

BillableP78.82

Peptic ulcer of newborn

BillableP78.83

Newborn esophageal reflux

BillableP78.84

Gestational alloimmune liver disease

Billable
Also Known As / Clinical Terms(99)

SNOMED CT

UMLS

Clinical Terms

  • Cholestasis in newborn
  • PP - Pneumoperitoneum
  • PFIC2 - progressive familial intrahepatic cholestasis type 2
  • Perinatal pneumoperitoneum
  • Gastrointestinal hormone-secreting endocrine tumour
  • Transient neonatal colitis
  • NLRC4-related infantile enterocolitis, autoinflammatory syndrome
  • Neonatal hepatocellular damage
  • Haemophagocytic syndrome
  • Periodic fever, infantile enterocolitis, autoinflammatory syndrome
  • Neonatal malabsorption co-occurrent and due to gastrointestinal hormone-secreting endocrine tumour
  • Neonatal dermatitis
  • Macrophage activation syndrome
  • Hemophagocytic lymphohistiocytosis
  • Reactive haemophagocytic syndrome
  • Progressive familial intrahepatic cholestasis type 2
  • Neonatal oesophagitis
  • Familial intrahepatic cholestasis
  • Hyperinflammatory lymphohistiocytosis
  • Isolated neonatal sclerosing cholangitis
  • NLRC4-related macrophage activation syndrome
  • Haemophagocytic lymphohistiocytosis with rheumatologic disease
  • Gastritis of newborn
  • Dermatitis of the newborn
  • NLRC4-related autoinflammatory syndrome with macrophage activation syndrome
  • Sclerosing cholangitis
  • Neonatal malabsorption with gastrointestinal hormone-secreting endocrine tumor
  • Haemophagocytic lymphohistiocytosis
  • Esophagitis in newborn
  • Hemophagocytic syndrome
  • Hepatocellular liver damage
  • Neonatal esophagitis
  • Progressive familial intrahepatic cholestasis
  • PFIC - progressive familial intrahepatic cholestasis
  • Gastrointestinal hormone-secreting endocrine tumor
  • BSEP (bile salt export pump) deficiency
  • Neonatal malabsorption co-occurrent and due to gastrointestinal hormone-secreting endocrine tumor
  • Progressive intrahepatic cholestasis
  • Hemophagocytic lymphohistiocytosis with rheumatologic disease
  • Neonatal cholestasis
  • Reactive hemophagocytic syndrome
  • Pneumoperitoneum
  • Neonatal inflammatory skin and bowel disease
  • Peritoneal cavity free air
  • Disorder of oral mucosa in neonate
  • Neonatal disorder of oral mucosa
  • Fatal intrahepatic cholestasis
  • Inflammatory dermatosis of newborn
  • Neonatal malabsorption with gastrointestinal hormone-secreting endocrine tumour
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.

How does P78.89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified perinatal digestive system disorders 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 P78.89?

There is no direct ICD-11 mapping available for P78.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.