Genetic Testing for Hereditary Pancreatitis - CAM 309HB

Pancreatitis is defined as inflammation of the pancreas that progresses from acute (AP) (sudden onset; duration < 6 months) to recurrent acute (RAP) (> 1 episode of acute pancreatitis) to chronic (CP) (duration > 6 months) (LaRusch et al., 2014). This recurrent inflammation can lead to total destruction of the pancreas with subsequent pancreatic insufficiency, secondary diabetes, increased risk for pancreatic cancer, and severe unrelenting pain (Ravi Kanth & Nageshwar Reddy, 2014). Hereditary pancreatitis is the early onset form of chronic pancreatitis that is carried in an autosomal dominant pattern with variable penetrance (LaRusch et al., 2012). 

Application of coverage criteria is dependent upon an individual’s benefit coverage at the time of the request.

  1. For individuals under 20 years of age, genetic testing for hereditary pancreatitis (see Note 1) is considered MEDICALLY NECESSARY when at least one of the following conditions is met:
    1. For individuals with recurrent (two separate, documented episodes with hyperlipasemia) attacks of acute pancreatitis for which there is no identifiable cause.
    2. For individuals with unexplained chronic pancreatitis.
    3. For individuals with a first- or second-degree relative (see Note 2) with a history of recurrent acute pancreatitis, idiopathic chronic pancreatitis, or childhood pancreatitis without a known cause.
    4. For individuals with an unexplained episode of pancreatitis that required hospitalization.

The following does not meet coverage criteria due to a lack of available published scientific literature confirming that the test(s) is/are required and beneficial for the diagnosis and treatment of an individual’s illness.

  1. For all other situations not described above, genetic testing for hereditary pancreatitis is considered NOT MEDICALLY NECESSARY.


Note 1: For 5 or more gene tests being run on the same platform, please refer to CAM 235 Reimbursement Policy.

Note 2: First-degree relatives include parents, full siblings, and children of the individual. Second-degree relatives include grandparents, aunts, uncles, nieces, nephews, grandchildren, and half-siblings of the individual.

Pancreatitis is caused by unregulated trypsin activity within the pancreatic acinar cell or pancreatic duct that leads to pancreatic autodigestion and pancreatic inflammation (Lerch & Gorelick, 2000; Whitcomb, 1999). Under acinar cell stress (e.g., hyperstimulation, intracellular hypercalcemia), intracellular trypsinogen is likely converted to trypsin, which activates other digestive enzymes causing injury. Injury releases immune system-activating molecules that cause an initial acute inflammatory response, followed by recruitment of tissue macrophages and activated pancreatic stellate cells. Recurrent injury leads to chronic pancreatitis and fibrosis, mediated by pancreatic stellate cells (Werlin et al., 2015).

Chronic pancreatitis (CP) is a progressive inflammatory disease in which the pancreatic tissue is destroyed over time and replaced by fibrous tissue. The process of fibrosis usually leads to progressive worsening in the structural integrity of the pancreas, changes in arrangement, and composition of the islets, and deformation of the large ducts, eventually resulting in the impairment of both exocrine and endocrine functions (Brock et al., 2013). The annual incidence of the disease has been estimated to be 5 – 10 per 100,000 persons (Molven et al., 2015). The main symptom of CP is pain; however, it is highly variable in character, frequency, and severity (Mullady et al., 2011; Whitcomb et al., 2008). Therapeutic efforts are mostly aimed at extracting stones and decompressing pancreatic ducts to achieve ideal drainage of the pancreatic duct (Li et al., 2010; Tandan & Nageshwar Reddy, 2013). Genetic risk factors play a larger role in early-onset CP as opposed to late-onset CP. Older adults have a host of environmental and genetic factors that contribute to CP development while hereditary pancreatitis is postulated to make up less than 4% of CP in late-onset groups (Wertheim-Tysarowska et al., 2021). 

The etiologies of chronic pancreatitis are classified by the TIGAR-O system into alcoholism, hyperlipidemia, obstructive damage caused by trauma or congenital anomalies, hereditary pancreatitis, autoimmune pancreatitis, and idiopathic (Etemad & Whitcomb, 2001; Sun et al., 2015). The genetic factors listed in TIGAR-O are PRSS1 (listed as “cationic trypsinogen”), CFTR, SPINK1, and alpha-1-antitrypsin (listed as “possible”) (Etemad & Whitcomb, 2001). TIGAR-O Version 2 was published in 2019, and lists PRSS1, CFTR, SPINK1, CTRC, CASR, and CEL as genetic factors, as well as some modifier genes such as CLDN2 (Whitcomb, 2019).

Hereditary pancreatitis (HP) presents as an autosomal dominant chronic pancreatitis with variable penetrance. It mainly develops in childhood (Wertheim-Tysarowska et al., 2021). This variability has been attributed to a genetic predisposition to chronic pancreatitis with the additive effects of environmental and inherited factors. Most genes associated with HP either directly encode components of the trypsin system of the exocrine pancreas or are likely to perturb this system indirectly. HP is recognized when pathogenic gene variants of the PRSS1 gene are found or when acute or chronic pancreatitis develops with a distinct family history (Wertheim-Tysarowska et al., 2021). The phenotype of HP is increased susceptibility to acute pancreatitis, resulting in chronic pancreatitis (including pancreatic fibrosis, chronic pain, maldigestion, and diabetes mellitus) occurring in at least 50%. The risk of pancreatic cancer is also increased (Whitcomb, 2021). 

Genes Linked to Hereditary Pancreatitis
PRSS1 encodes trypsin-1 (cationic trypsinogen), a major pancreatic digestive enzyme. Mutations in PRSS1 typically result in a trypsin protein that is either prematurely activated or resistant to degradation (LaRusch et al., 2012; Masson et al., 2008), causing autosomal dominant pancreatitis in 60% – 100% of families with hereditary pancreatitis (LaRusch & Whitcomb, 2011). “The age of onset for PRSS-1 related HP ranges from 10 to 12 years” (Hasan et al., 2018). 

SPINK1 encodes serine protease inhibitor, Kazel-type 1, a trypsin inhibitor that is upregulated by inflammation (Grendell, 2003). It is not a typical susceptibility gene for acute pancreatitis, but rather a susceptibility gene for the chronic pancreatitis that follows acute pancreatitis.

CTRC encodes chymotrypsin C. Prematurely activated trypsin is destroyed by CTRC by acting on the molecule within the calcium-binding loop in the absence of calcium and, therefore, is a crucial candidate gene in the pathogenesis of pancreatitis (Szmola & Sahin-Toth, 2007).

CASR encodes calcium sensing receptor, mutations of which can cause increased calcium ion levels increasing trypsin activation and failed trypsin degradation (Whitcomb, 2004).

CFTR encodes the cystic fibrosis transmembrane conductance protein. Mutations are associated with recurrent acute and chronic pancreatitis since dysfunctional CFTR can result in retention of zymogens that can become active and result in pancreatitis (LaRusch & Whitcomb, 2011).

CLDN2 encodes claudin-2, a tight-junction protein that seals the space between epithelial cells. Normally expressed in the proximal pancreatic duct, CLDN2 is thought to facilitate the transport of water and sodium into the duct to match the chloride and bicarbonate that are actively secreted by pancreatic duct cells through CFTR. It is strongly associated with alcohol-related chronic pancreatitis rather than recurrent acute pancreatitis (Ravi Kanth & Nageshwar Reddy, 2014).

CPA1 encodes carboxypeptidase A1; mutated CPA1 is associated with nonalcoholic chronic pancreatitis, especially with an early age of onset (Witt et al., 2013). Risk for chronic pancreatitis unrelated to trypsin activation appears to be related to endoplasmic reticulum stress from pathogenic CPA1 variants that alter protein folding, triggering the unfolded protein response.

MYO9B gene and the two tight-junction adaptor genes, PARD3 and MAGI2, have been linked to gastrointestinal permeability. Impairment of the mucosal barrier plays an important role in the pathophysiology of acute pancreatitis (Nijmeijer et al., 2013).

CEL encodes carboxyl-ester lipase, and CEL mutations can cause an autosomal dominant syndrome of maturity-onset diabetes of the young (MODY) and exocrine pancreatic dysfunction (Molven et al., 2015).

TRPV6 is a potential novel susceptibility gene for CP that plays a role in epithelial calcium absorption and reabsorption. Variants of this gene also co-occur with pathogenic variants of genes such as SPINK1 and CFTR (Wertheim-Tysarowska et al., 2021).

Disorder(s) Genetic Cause(s) Consequence(s) Source Citation

Shwachman-Diamond syndrome

SBDS, DNAJC21, EFL1, and SRP54

affect RNA function

(Nelson & Myers, 2008)

Mitochondrial (mt)DNA deletion syndromes, including Kearns-Sayre syndrome (KSS), Pearson syndrome, and progressive external ophthalmoplegia (PEO)  

Multiple possible mitochondrial genetic etiologies, including SLC25A4, TWNK, POLG, TYMP, OPA1, RRM2B, DNA2, and MT-TL1,

defective oxidative phosphorylation

(Goldstein & Falk, 2003)

Carboxyl ester lipase (CEL-MODY)


pancreatic exocrine, endocrine dysfunction, and chronic pancreatitis

(O'Neill et al., 2013)

Johanson-Blizzard syndrome


protein synthesis

(Kniffin & McKusick, 2012)









Syndromes that Include Pancreatitis or Pancreatic Insufficiency

Several genes are associated with rare disorders in which pancreatitis or pancreatic insufficiency is part of their phenotype (Durie, 1996; Lerch et al., 2006).
As the number of genes and mutations involved in the onset and progression of pancreatitis becomes higher (Ooi et al., 2010; Walker et al., 2013), the time and cost of screening and sequencing specific genes continues to increase. However, massive parallel sequencing or next generation sequencing (NGS) is becoming standardized (Ballard et al., 2015), and the cost per patient is rapidly dropping (Palermo et al., 2016). NGS includes whole genome sequencing, whole exome sequencing (WES) and other methods. Because the cost of WES is now less than the cost of sequencing CFTR, use of this technology is becoming an attractive alternative to classic targeted gene sequencing or mutation specific genotyping for a genetic counseling workup (LaRusch et al., 2012). In response to this accelerating development of sequencing techniques, several firms have created genetic panels focusing on hereditary pancreatitis. For example, Invitae offers a six-gene panel (CASR, CFTR, CPA1, CTRC, PRSS1, SPINK1) for chronic pancreatitis (Invitae, 2023). Other firms offering proprietary panels include ARUP Laboratories (4 genes), LabCorp (3 genes), and Ambry (6 genes) (Ambry, 2023; ARUP, 2023; LabCorp, 2023). Still other firms evaluate as many as 12 genes and more (Whitcomb, 2021).

Clinical Utility and Validity
Testing for mutations in the PRSS1, SPINK, and CFTR genes is usually done by either direct sequence analysis or next generation sequencing, both of which have high analytic validity. Several studies have evaluated the clinical validity of genetic testing (Applebaum-Shapiro et al., 2001; Ceppa et al., 2013; Poddar et al., 2015; Sultan et al., 2012). One limitation with some studies was lack of inclusion of patients with clinically defined hereditary pancreatitis. Hence, the true clinical sensitivity and specificity of genetic testing in hereditary pancreatitis cannot be accurately determined and needs to be further researched. Similarly, there is a lack of published literature on the clinical utility of testing. Further research is required to evaluate how genetic testing will impact patient management decision and clinical outcomes.

Kumar et al. (2016) sought to characterize and identify risk factors associated with acute recurrent pancreatitis (ARP) and CP in childhood in a multinational cross-sectional study (INSPPIRE). The authors analyzed 301 children with ARP or CP. They found that “At least 1 gene mutation in pancreatitis-related genes was found in 48% of patients with ARP vs 73% of patients with CP. Children with PRSS1 or SPINK1 mutations were more likely to present with CP compared with ARP (PRSS1: OR = 4.20 and SPINK1: OR = 2.30). Obstructive risk factors presented in 33% in both groups, but toxic/metabolic risk factors were more common in children with ARP (21% overall; 26% ARP, 15% CP). They concluded that “The high disease burden in pediatric CP underscores the importance of identifying predisposing factors for progression of ARP to CP in children” (Kumar et al., 2016).

Grabarczyk et al. (2017) also found that CTRC variants are strong CP risk factors in pediatric patients. The authors investigated 136 pediatric patients with CP and compared them to 401 controls. They showed that p.Arg254Trp (4.6%) and p.Lys247_Arg254del (5.3%) heterozygous mutations are frequent and significantly associated with CP risk in pediatric patients (odds ratio [OR] = 19.1; 95% CI 2.8 – 160; P = 0.001 and OR = 5.5; 95% CI 1.6 – 19.4; P = 0.001, respectively). The c.180TT genotype of common p.Gly60Gly variant was found to be a strong and independent CP risk factor (OR = 23; 95% CI 7.7 – 70; P <  0.001) with effect size comparable to p.Arg254Trp mutation (Grabarczyk et al., 2017).

Schwarzenberg et al. (2015) evaluated the genetic spectrum of CP. 76 CP patients were examined, and 51 were found to have a genetic risk factor for CP. Of these 51 mutations, 33 were a PRSS1 mutation, 14 were a SPINK1 mutation, 11 were a CFTR mutation, and 2 were a CTRC mutation. The final 25 patients were found to have an obstructive risk factor (Schwarzenberg et al., 2015).

Zou et al. (2018) evaluated the prevalence of four CP-related genes (SPINK1, PRSS1, CTRC, CFTR) in Han Chinese patients. The authors performed next-generation sequencing on 1061 patients and 1196 controls. The 1061 patients were further divided into three categories, idiopathic CP (ICP, 715 patients), alcoholic CP (ACP, 206), and smoking-associated CP (SCP, 140). The impact of rare pathogenic variants on age of onset and clinical outcomes was evaluated. Rare pathogenic variants were found in 535 CP patients compared to 71 controls. Mutation positive patients were found to have earlier age of onset as well additional clinical features such as pancreatic stones and diabetes mellitus compared to mutation negative ICP patients. Overall, pathogenic variants were found in 57.1% of ICP patients, compared to 39.8% of ACP patients and 32.1% of SCP patients. The authors concluded that rare pathogenic variants “significantly” influenced age of onset and clinical outcomes of CP (Zou et al., 2018).

Nabi et al. (2020) evaluated 239 children in a prospective study from January 2015 to May 2018 to examine genetic risk factors in children with idiopathic acute recurrent pancreatitis (IARP). Among the enrollees, 85.35% children had IARP, and found that family history of pancreatitis was found among 4.6% of participants. For specific genes, “mutations/polymorphisms in at least 1 gene were identified in 89.5% (129/144) children including SPINK1 in 41.9%, PRSS1 (rs10273639) in 58.2%, CTRC in 25.6%, CTSB in 54.9%, CLDN2 in 72.9%, and CFTR in 2.3%.” This conveys the overlapping genetic nature of IARP with related genes in HP, making genetic testing important for managing potential disease progression. 

Suzuki et al. (2020) investigated the currently understood genetic abnormalities in pancreatitis, and found that “patients with these genetic predispositions [PRSS1 and SPINK1 genes], both children and adults, have often been initially diagnosed with idiopathic acute pancreatitis, in approximately 20 – 50% pediatric cases and 28 – 0% of adult cases… Patients with chronic pancreatitis (CP) due to SPINK1 gene mutation and HP patients have a potentially high risk of pancreatic exocrine insufficiency, diabetes mellitus, and of particular importance, pancreatic cancer.” This conveys the continuously emphasized clinical utility of genetic testing to pursue opportunities for counselling and symptom management with disease progression, despite not having gene therapy options for directly targeting HP causing and associated genes (Suzuki et al., 2020).

Weiss et al. (2020) discussed the potential pitfalls from using next generation sequencing (NGS) to diagnose PRSS1 mutations in chronic pancreatitis. Due to the “high degree of DNA sequence homology (> 91%) between PRSS1 and other members of the trypsinogen multigene family,” there may be erroneous diagnoses of pathologic chronic pancreatitis among patients with benign variants of other PRSS1- related genes, like PRSS2 or PRSS3P2. The researchers concluded that sequence homology “can confound the mapping of short NGS reads to a reference genome and lead to technical artefacts.” They recommend “careful clinical evaluation, pretest and post-test genetic counselling and confirmation of NGS test results by Sanger sequencing” to confirm a diagnosis of genetically mutated chronic pancreatitis. This presented the precautions that must be accounted for when utilizing genetic testing for hereditary pancreatitis (Weiss et al., 2020).

Zou et al. (2020) performed whole genome sequencing on a population of 464 Chinese CP patients and on a group of 504 control participants. The Transient receptor potential cation channel, Subfamily V, Member 6 (TRPV6) gene was identified as a gene significantly associated with chronic pancreatitis through a “burden test of aggregated rare nonsynonymous variants with a combined annotation dependent depletion score > 20 (p = .020).” In another phase of the study, Sanger sequencing was used to analyze the entire coding sequence and exon/intron boundaries of the TPRV6 gene. Combining the two phases of the study, the authors identified 25 distinct variants of TPRV6 and noted that loss-of-function variants were over-represented in the chronic pancreatitis group. The authors concluded that TPRV6 is likely a novel susceptibility gene for chronic pancreatitis.

A Consensus Committees of the European Registry of Hereditary Pancreatic Diseases, the Midwest Multi-Center Pancreatic Study Group and the International Association of Pancreatology developed guidelines for genetic testing of the PRSS1 gene and genetic counseling for HP (Ellis et al., 2001). The recommended indications for symptomatic patients included: 

  • Recurrent (two separate, documented episodes with hyperlipasemia) attacks of acute pancreatitis for which there is no explanation (anatomical anomalies, ampullary or main pancreatic strictures, trauma, viral infection, gallstones, alcohol, drugs, hyperlipidaemia, etc.).
  • Unexplained chronic pancreatitis.
  • A family history of pancreatitis in a first- or second-degree relative.
  • Unexplained episode of pancreatitis in a child that required hospitalization.

Predictive (presymptomatic) genetic testing of unaffected relatives is considered more complex. Predictive testing is recommended only for individuals with a first-degree relative with a defined HP gene mutation, and who are over 16 years of age and capable of making an independent and fully informed decision (Ellis et al., 2001). 

American Society of Clinical Oncology (ASCO)
ASCO states that “genetic testing is sometimes considered for patients who develop recurrent pancreatitis at young ages. Genetic testing is available for mutations in the PRSS1, SPINK1, and CFTR genes” (ASCO, 2022).

American College of Gastroenterology (ACG) 
In 2013, the ACG issued guidelines for the management of acute pancreatitis. They include the following recommendation: “genetic testing may be considered in young patients (< 30 years old) if no cause is evident and a family history of pancreatic disease is present (conditional recommendation, low quality of evidence).” ACG also states that “the role of genetic testing in AP has yet to be determined, but may be useful in patients with more than one family member with pancreatic disease. Individuals with IAP and a family history of pancreatic diseases should be referred for formal genetic counseling” (Tenner et al., 2013).

In 2020, the ACG published an update on chronic pancreatitis. In it, they recommend genetic testing in patients “with clinical evidence of a pancreatitis-associated disorder or possible CP [chronic pancreatitis] in which the etiology is unclear, especially in younger patients (strong recommendation, low quality of evidence).” The guideline goes on to state that “at minimum, patients with idiopathic CP should be evaluated for PRSS1, SPINK1, CFTR, and CTRC gene mutation analysis …” The guideline mentions that assessment of germline mutations is primarily for prognostic and therapeutic purposes, rather than diagnostic (Gardner et al., 2020).

United European Gastroenterology
The United European Gastroenterology published evidence-based guidelines for the diagnosis and therapy of chronic pancreatitis which recommend (Lohr et al., 2017):

“All patients with a family history or early onset disease (< 20 years) should be offered genetic testing for associated variants.”

“Genetic screening for every CP patient cannot be recommended since alcohol abuse is the predominant cause of the disease in up to 60% of adult cases.” 

“In patients with early onset CP, genetic screening can be offered after informed consent.”

“In patients with alcoholic CP, routine genetic testing cannot be recommended.”

The working group also noted that “variants in SPINK1 and CTRC, and to a lesser extent, common single-nucleotide polymorphisms (SNPs) in the PRSS1 and CLDN2-MORC4 loci, are associated with alcoholic CP” (Lohr et al., 2017).

European Pancreatic Club/ Hungarian Pancreatic Study Group 
The European Pancreatic Club, in collaboration with the Hungarian Pancreatic Study Group organized a consensus guideline meeting on the diagnosis and management of pancreatitis in the pediatric population which state (Parniczky et al., 2018):

“Pediatric AP and RAP often develop in the background of genetic susceptibility and genetic testing is warranted in patients with a second episode of idiopathic AP or first episode of idiopathic AP and a family history of AP or CP. Full sequence analysis of PRSS1, SPINK1, CTRC, CPA1 and CFTR gene exons and exon-intron boundaries and testing for the pathogenic CEL hybrid allele are recommended.”

“Variants in the PRSS1 and CPA1 genes may be associated with a family history of pancreatitis or even autosomal dominant hereditary pancreatitis. Children with a single episode of AP are at risk for developing a second episode. However, genetic testing is cumbersome and expensive. There is usually no therapeutic consequence, but it may assist in long term prognosis.”

“The presence of mutations in the above mentioned genes increases the risk of ARP and CP. Hereditary pancreatitis associated with mutations in PRSS1, especially p.R122H, that could considerably increase the risk of pancreatic adenocarcinoma. Knowing the genetic risk factors may not alter the therapy, but it helps to understand the disease's etiological background for the disease and may lead to future targeted investigation” (Parniczky et al., 2018).

International Study Group of Pediatric Pancreatitis: In search for a cuRE (INSPPIRE) Consortium 
This group was formed “to collect detailed information on a cohort of children with ARP and CP with the aim to fill gaps in knowledge and improve clinical care.” Their genetic testing-related guidelines are listed below:

  • “The search for a genetic cause of ARP or CP should include a sweat chloride test (even if newborn screening for cystic fibrosis (CF) is negative) and PRSS1 gene mutation testing. Genetic testing for CF should be considered if a sweat test is unable to be performed.”
  • “Mutation analysis of the genes SPINK1, CFTR and CTRC may identify risk factors for ARP or CP.”
  • “Patients with ARP or CP and a sweat test < = 60 mmol/L should have expanded CFTR mutation testing done if there is no other identified cause of their pancreatic disease (such as a PRSS1 mutation or a clear obstructive etiology)” (Gariepy et al., 2017).

National Comprehensive Cancer Network (NCCN)
The NCCN notes familial pancreatitis and non-hereditary forms of pancreatitis are both linked with an increased risk of pancreatic cancer. Additionally, chronic pancreatitis is another risk factor for pancreatic cancer. The NCCN specifically lists PRSS1, SPINK1, and CFTR as contributing genes to familial pancreatitis. The approximate increase in risk of pancreatic cancer is somewhere between 26-fold and 87-fold in those with the PRSS1, SPINK1, and CFTR gene mutations (NCCN, 2023).

International Association of Pancreatology, American Pancreatic Association, Japan Pancreas Society, and European Pancreatic Club
In 2020, the International Association of Pancreatology, the American Pancreatic Association, the Japan Pancreas Society, and European Pancreatic Club released a set of international consensus guidelines on surveillance for pancreatic cancer in the setting of chronic pancreatitis. Though the working group did not explicitly endorse or oppose genetic testing, it was clear that due to the recommendations separated by genetic variants within chronic pancreatitis, genetic testing would become critical for surveillance. With regards to the conditions by which hereditary pancreatitis would warrant surveillance for cancer, the working group stated: 

  • “The risk of pancreatic cancer in affected individuals with an autosomal dominant history of hereditary pancreatitis due to inherited PRSS1 mutations is high enough to justify surveillance. Quality assessment: high; recommendation: strong”
  • “The risk of pancreatic cancer in affected individuals with an autosomal dominant history of hereditary pancreatitis but without PRSS1 mutations is high enough to justify surveillance. Quality assessment: moderate; recommendation: weak”
  • “The risk of pancreatic cancer in patients with chronic pancreatitis associated with SPINK1 p. N34S is not high enough to justify screening or surveillance. Quality assessment: moderate; recommendation: strong”
  • “The risk of pancreatic cancer in patients with chronic pancreatitis associated with other germline mutations including those of CFTR, CTRC, CPA1, and CEL, is not high enough to justify screening or surveillance. Quality assessment: moderate; recommendation: conditional” (Greenhalf et al., 2020).

National Institute for Health and Care Excellence (NICE) 
NICE updated their guidelines on pancreatitis in December 2020. With regards to genetic testing for hereditary pancreatitis (acute) and patient information, NICE stated the following: 

“Give people with pancreatitis, and their family members or carers (as appropriate), written and verbal information on the following, where relevant, as soon as possible after diagnosis:

  • Pancreatitis and any proposed investigations and procedures, using diagrams
  • Hereditary pancreatitis, and pancreatitis in children, including specific information on genetic counselling, genetic testing, risk to other family members, and advice on the impact of their pancreatitis on life insurance and travel
  • The long-term effects of pancreatitis, including effects on the person's quality of life
  • The harm caused to the pancreas by smoking or alcohol"

For an individual with chronic pancreatitis, NICE recognizes that the cause may not be alcohol-related, but can include “genetic factors; autoimmune disease, in particular IgG4 disease; metabolic causes; [and] structural or anatomical factors” (NICE, 2020).

Table of Terminology




American College of Gastroenterology


Acute pancreatitis


Acute recurrent pancreatitis


Associated Regional and University Pathologists, Inc. 


American Society of Clinical Oncology


Calcium sensing receptor


Carboxyl ester lipase


Cystic fibrosis


Cystic fibrosis transmembrane conductance regulator




Chronic pancreatitis


Carboxypeptidase A1


Chymotrypsin C


Deoxyribonucleic acid 


Deoxyribonucleic acid replication helicase/nuclease 2


Deoxyribonucleic acid J heat shock protein family (Hsp40) member C21


Elongation factor like-1


European Pancreatic Club


Hereditary pancreatitis


Hungarian pancreatic study group


Idiopathic acute pancreatitis


International Study Group of Pediatric Pancreatitis


Kearns-Sayre syndrome


Membrane-associated Guanylate Kinase Inverted-2


Maturity-onset diabetes of the young




Myosin IXB


North American Pancreatitis Study 2


National Comprehensive Cancer Network


Next generation sequencing


Mitochondrial dynamin


Odds ratio


Partitioning defective 3


Progressive external ophthalmoplegia


DNA polymerase subunit gamma


Cationic trypsinogen


Recurrent acute


Ribonucleotide-diphosphate reductase subunit M2


Shwachman-Bodian-Diamond Syndrome


Smoking-associated chronic pancreatitis


Solute carrier family 25 member 4


Serine protease inhibitor


Pancreatic secretory trypsin inhibitor Kazal type 1


Toxic-Metabolic; Idiopathic; Genetic; Autoimmune; Recurrent and Severe Acute Pancreatitis; Obstructive


Twinkle mitochondrial deoxyribonucleic acid helicase


Thymidine phosphorylase


Whole exome sequencing


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Coding Section






CFTR (cystic fibrosis transmembrane conductance regulator) (e.g., cystic fibrosis) gene analysis; duplication/deletion variants 



CFTR (cystic fibrosis transmembrane conductance regulator) (e.g., cystic fibrosis) gene analysis; full gene sequence



CFTR (cystic fibrosis transmembrane conductance regulator) (e.g., cystic fibrosis) gene analysis; intron 8 poly-T analysis (e.g., male infertility)



Molecular pathology procedure, Level 2 (e.g., 2 – 10 SNPs, 1 methylated variant, or 1 somatic variant [typically using nonsequencing target variant analysis], or detection of a dynamic mutation disorder/triplet repeat)



Molecular pathology procedure, Level 5 (e.g., analysis of 2 – 5 exons by DNA sequence analysis, mutation scanning or duplication/deletion variants of 6 – 10 exons, or characterization of a dynamic mutation disorder/triplet repeat by Southern blot analysis)



Molecular pathology procedure, Level 6 (e.g., hereditary pancreatitis), full gene sequence 



Unlisted molecular pathology procedure

ICD-9-CM Diagnosis


Acute pancreatitis



Chronic pancreatitis

ICD-10-CM (effective 10/01/15)


Acute pancreatitis code range



Other chronic pancreatitis

ICD-10-PCS (effective 10/01/15)


Not applicable. ICD-10-PCS codes are only used for inpatient services. There are no ICD procedure codes for laboratory tests.

Type of Service



Place of Service



Procedure and diagnosis codes on Medical Policy documents are included only as a general reference tool for each policy. They may not be all-inclusive.

This medical policy was developed through consideration of peer-reviewed medical literature generally recognized by the relevant medical community, U.S. FDA approval status, nationally accepted standards of medical practice and accepted standards of medical practice in this community, Blue Cross Blue Shield Association technology assessment program (TEC) and other nonaffiliated technology evaluation centers, reference to federal regulations, other plan medical policies, and accredited national guidelines.

"Current Procedural Terminology © American Medical Association. All Rights Reserved" 

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