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Test ID: VHLZ VHL Gene, Full Gene Analysis, Varies

Useful For

Diagnosis of suspected von Hippel-Lindau (VHL) disease


Diagnosis of suspected VHL-related hereditary erythrocytosis

Method Name

Polymerase Chain Reaction (PCR) Followed by DNA Sequence Analysis and Gene Dosage Analysis by Multiplex Ligation-Dependent Probe Amplification (MLPA)

Reporting Name

VHL Gene, Full Gene Analysis

Specimen Type


Shipping Instructions

Specimen preferred to arrive within 96 hours of draw.

Specimen Required

Patient Preparation: A previous bone marrow transplant from an allogenic donor will interfere with testing. Call 800-533-1710 for instructions for testing patients who have received a bone marrow transplant.

Specimen Type: Whole blood


Preferred: Lavender top (EDTA) or yellow top (ACD)

Acceptable: Any anticoagulant

Specimen Volume: 3 mL

Collection Instructions:

1. Invert several times to mix blood.

2. Send specimen in original tube.

Specimen Minimum Volume

1 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Varies Ambient (preferred)

Clinical Information

von Hippel-Lindau (VHL) disease is an autosomal dominant cancer predisposition syndrome with a prevalence of approximately 1 in 36,000 livebirths. It predisposes affected individuals to the development of mainly 5 different types of neoplasms: retinal angioma (approximately 5%-70% penetrance), cerebellar hemangioblastoma (CHB) (44%-72% penetrance), clear-cell renal cell carcinoma (cRCC) (approximately 25%-60% penetrance), spinal hemangioblastoma (SHB) (approximately 13%-50% penetrance), and pheochromocytoma (PC) (approximately 10%-20% penetrance). Angiomas in other organs, pancreatic cysts/adenomas/carcinomas, islet cell tumors, and endolymphatic sac tumors can also occur. VHL-related tumors typically present in the second to third decade of life, but sometimes earlier, particularly for retinal angiomas. For each tumor type, the incidence rates rise steadily, albeit at different slopes, throughout life.


VHL disease is caused by heterozygous germline loss-of-function sequence variants, small deletions or insertions (approximately 80% of cases), or large germline deletions (approximately 20% of cases) of the VHL gene. Approximately 20% of cases are due to new (de novo) pathogenic variants, which in some cases result in disease mosaicism. This presents a diagnostic challenge for individuals who present with clinical signs of VHL disease, but test negative genetically because the pathogenic variant is not present in all peripheral leukocytes.


VHL encodes the VHL protein, a tumor suppressor protein that is involved in ubiquitination and degradation of a variety of other proteins, most notably hypoxia-inducible factor (HIF). HIF induces expression of genes that promote cell survival and angiogenesis under conditions of hypoxia. It is believed that diminished HIF degradation due to inactive VHL protein causes the tumors in VHL disease. Tumors form when the remaining intact copy of VHL is somatically inactivated in target tissues (2-hit model). Sporadic cRCC, unrelated to VHL disease, also shows somatic deletions, sequence variants, or aberrant methylation in 80% to 100% of cases.


Retinal angioma, CHB, and SHB cause morbidity and some mortality through pressure on adjacent structures and through retinal or subarachnoid hemorrhages. VHL-related cRCC and PC follow a similar clinical course as their sporadic counterparts, with substantial morbidity and mortality. Early detection of VHL-related tumors can reduce these adverse outcomes, and surveillance of affected individuals is, therefore, widely advocated. Genetic testing is the most accurate way to identify presymptomatic individuals, who can then be entered into a surveillance program.


Research has suggested that certain combinations of VHL tumors cluster in VHL families, and this may be driven by the type of VHL gene variant present in the family. This observation has led to a phenotype-based classification of VHL syndrome. However, it should be noted that these patterns are not clear cut, and should not necessarily be used for diagnostic or therapeutic purposes.


VHL Type 1: Retinal angioma, central nervous system (CNS) hemangioblastoma, renal cell carcinoma, pancreatic cysts, and neuroendocrine tumors. Low risk for pheochromocytoma. Associated with pathogenic truncating or missense variants that are predicted to grossly disrupt the folding of VHL protein.


VHL Type 2: Pheochromocytoma, retinal angiomas, and CNS hemangioblastoma. High risk for pheochromocytoma. Associated with pathogenic missense variants.


VHL Type 2 is further subdivided:

-Type 2A: Pheochromocytoma, retinal angiomas, and CNS hemangioblastomas; low risk for renal cell carcinoma

-Type 2B: Pheochromocytoma, retinal angiomas, CNS hemangioblastomas, pancreatic cysts, and neuroendocrine tumor; high risk for renal cell carcinoma

-Type 2C: Risk for pheochromocytoma only


Additionally, pathogenic sequence variants distinct from those associated with VHL syndrome can cause hereditary erythrocytosis or polycythemia. Cases of VHL disease and erythrocytosis are largely mutually exclusive, and patients who present with erythrocytosis do not typically develop the neoplasms discussed above, although they are sometimes associated with varicose veins and vertebral hemangiomas. Erythrocytosis due to VHL is caused by germline homozygous or compound heterozygous pathogenic sequence variants, and is inherited in an autosomal recessive manner. These patients usually have a markedly high erythropoietin level in the presence of an elevated hematocrit. Erythrocytosis due to a germline homozygous missense variant at nucleotide c.598C->T, p.R200W in the VHL gene has been found endemically in the Chuvash region of Russia, leading individuals with this variant to be labeled as having Chuvash polycythemia (CP), although further studies have determined that this variant can be found in other ethnic groups as well. These patients are at an increased risk to develop cerebrovascular and embolic complications. Heterozygous carriers are typically unaffected.

Reference Values

An interpretive report will be provided.


Evaluation and categorization of variants is performed using the most recent published American College of Medical Genetics recommendations as a guideline.(1) Variants are classified based on known, predicted, or possible pathogenicity and reported with interpretive comments detailing their potential or known significance.


Multiple in silico evaluation tools may be used to assist in the interpretation of these results. The accuracy of predictions made by in silico evaluation tools is highly dependent upon the data available for a given gene, and predictions made by these tools may change over time. Results from in silico evaluation tools should be interpreted with caution and professional clinical judgment.

Clinical Reference

1. Richards S, Aziz N, Bale S, et al: Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015;17:405-423

2. Online Mendelian inheritance in Man-OMIM. Available at

3. Universal Mutation database-UMD-VHL mutations database page. Available at

4. Maher ER, Kaelin WG Jr: von Hippel-Lindau disease (Reviews in Molecular Medicine). Medicine 1997;76:381-391

5. Pack SD, Zbar B, Pak E, et al: Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization. Cancer Res 1999;59:5560-5564

6. Richards FM: Molecular pathology of von Hippel-Lindau disease and the VHL tumor suppressor gene. Expert Rev Mol Med 2001;3:1-27

7. Hes FJ, Hoppener JW, Lips CJ: Clinical review 155: pheochromocytoma in von Hippel-Lindau disease. J Clin Endocrinol Metab 2003;88:969-974

8. Ong KR, Woodward ER, Killick P, et al: Genotype-phenotype correlations in von Hippel-Lindau disease. Hum Mutat 2007;28:143-149

9. Lonser RR, Glenn GM, McClellan W, et al: Von Hippel-Lindau disease. Lancet 2003;361:2059-2067

10. Stebbins CE, Kaelin WG, Pavletich NP: Structure of the VHL-ElonginC-ElonginB complex: implications for VHL tumor suppressor function. Science 1999;284:455-461

11. Frantzen C, Links TP, Giles RH: Von Hippel-Lindau Disease. In GeneReviews. Edited by RA Pagon, MP Adam, HH Ardinger, et al: University of Washington, Seattle. 1993-2015. 2000 May 17. Updated 2012 June 21. Available at

Day(s) Performed


Report Available

14 to 20 days

Test Classification

This test was developed, and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

81404-VHL (von Hippel-Lindau tumor suppressor) (eg, von Hippel-Lindau familial cancer syndrome), full gene sequence

81403-VHL duplication/deletion

LOINC Code Information

Test ID Test Order Name Order LOINC Value
VHLZ VHL Gene, Full Gene Analysis 82533-1


Result ID Test Result Name Result LOINC Value
37453 Result Summary 50397-9
37454 Result 82939-0
37455 Interpretation 69047-9
37456 Additional Information 48767-8
37457 Specimen 31208-2
37458 Source 31208-2
37459 Released By 18771-6


1. New York Clients-Informed consent is required. Document on the request form or electronic order that a copy is on file. The following documents are available in Special Instructions:

-Informed Consent for Genetic Testing (T576)

-Informed Consent for Genetic Testing-Spanish (T826)

2. VHL Gene Testing Patient Information (T641) in Special Instructions

3. If not ordering electronically, complete, print, and send an Oncology Test Request (T729) with the specimen.

Mayo Clinic Laboratories | Genetics and Pharmacogenomics Catalog Additional Information: