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Bulldog

Lifespan
9.8 years
95% CI 9.7 to 10 · McMillan 2024, n=11,065
Most carried variant
Cystinuria Type I-A
39% of 4,816 tested · Donner 2023
Behind this page
38 dogs
in the atlas · an early sketch · 4,816 tested for variants

Bulldogs have a cited life expectancy of 9.8 years (McMillan 2024 / VetCompass, n=11,065, 95% CI 9.7 to 10). The most carried tested variant is Cystinuria Type I-A, in 39% of 4,816 Bulldogs tested (Donner 2023), then Hyperuricosuria (18%) and Canine Multifocal Retinopathy 1 (14%). 38 dogs stand behind the atlas figures here, so treat this page as an early sketch.

Bulldog
Photo: Ultimoribelle · CC BY-SA 4.0 · Wikimedia

Also known as British Bulldog and English Bulldog.

Mendelian-disease genetics

What genetic diseases do Bulldogs carry?

From a panel of 250 Mendelian-disease variants screened in 1,054,293 dogs (Donner et al. 2023), Bulldogs carry 19 of them at observable frequency. Carrier frequency is not clinical risk. Most recessive variants require two copies for disease expression; many dominant variants show incomplete penetrance. Read this as a population fingerprint of what's in the gene pool, not a per-dog prediction.

high 39.4%
n = 4,816 dogs · 3 variants tested · OMIA:000256-9615 · omia.org →
SLC3A1what this gene does

SLC3A1 is a gene that helps transport certain amino acids in the kidneys. It plays a key role in preventing the buildup of cystine, which can form stones.

For your dog: If your dog is from a breed known to carry SLC3A1 variants, it’s worth discussing cystinuria risks with your vet, especially if urinary issues arise.

Hyperuricosuria (HUU)
Autosomal recessive
moderate 17.9%
n = 4,816 dogs · 1 variant tested · OMIA:001033-9615 · omia.org →
SLC2A9what this gene does

SLC2A9 is a gene that helps regulate uric acid levels in a dog's body. It plays a role in how the kidneys handle this substance.

For your dog: If your dog is one of the breeds known to carry this gene variant, it’s worth discussing with your vet to understand any potential urinary health concerns.

n = 4,816 dogs · 1 variant tested · OMIA:001444-9615 · omia.org →
BEST1what this gene does

BEST1 is a gene that helps maintain the health of the retina, the light-sensitive layer at the back of the eye. It plays a role in keeping the cells in the retina functioning properly.

For your dog: If your dog is from a breed known to carry BEST1 variants, it’s worth discussing retinal health with your vet, especially if you notice any vision changes.

Degenerative Myelopathy (DM)
Autosomal recessive (Incomplete penetrance)
moderate 12.7%
n = 4,816 dogs · 1 variant tested · OMIA:000263-9615 · omia.org →
SOD1what this gene does

SOD1 is a gene that helps protect cells from damage caused by harmful molecules called free radicals.

For your dog: If your dog is a carrier of SOD1 variants, it's worth discussing with your vet, but remember carrier status doesn't mean your dog will get the disease.

Cystinuria Type I-B (SLC7A9 p.A217T)
Autosomal recessive (Incomplete penetrance)
marker disputed 55.5%
n = 4,816 dogs · 2 variants tested · OMIA:001880-9615 · omia.org →
SLC7A9what this gene does

SLC7A9 is a gene that helps transport certain amino acids in the kidneys. It plays a role in how the body handles cystine, an amino acid that can form crystals.

For your dog: If your dog is a carrier, it’s worth discussing with your vet to monitor urinary health and catch any issues early.

n = 4,803 dogs · 1 variant tested · OMIA:000157-9615 · omia.org →
FGF4what this gene does

FGF4 influences leg length by affecting bone growth, leading to shorter legs in certain breeds.

For your dog: If your dog is from a breed known to carry this gene, it's worth discussing spinal health with your vet, but being a carrier doesn’t guarantee problems.

Factor VII Deficiency
Autosomal recessive
low 0.58%
n = 4,815 dogs · 1 variant tested · OMIA:000361-9615 · omia.org →
F7what this gene does

The F7 gene helps produce a protein important for blood clotting, which stops bleeding when dogs get injured.

For your dog: If your dog is from a breed known to carry F7 variants, it's worth mentioning to your vet before any surgery or if you notice unusual bleeding.

Cone-Rod Dystrophy (cord1-PRA/crd4)
Autosomal recessive (Incomplete penetrance)
low 0.20%
n = 4,808 dogs · 1 variant tested · OMIA:001432-9615 · omia.org →
RPGRIP1what this gene does

RPGRIP1 is a gene involved in the function of photoreceptor cells in the eye, which help dogs see in different light conditions.

For your dog: If your dog belongs to a breed known to carry RPGRIP1 mutations, it’s worth discussing with your vet to understand the risks and monitor eye health.

marker disputed 0.11%
n = 4,816 dogs · 2 variants tested · OMIA:000162-9615 · omia.org →
PDK4what this gene does

PDK4 helps regulate how cells use energy, especially in the heart muscle.

For your dog: If your dog is one of the breeds known to carry this gene, it’s worth discussing heart health with your vet, but being a carrier doesn’t mean your dog will develop disease.

n = 4,816 dogs · 1 variant tested · OMIA:001980-9615 · omia.org →
n = 4,816 dogs · 1 variant tested · OMIA:001402-9615 · omia.org →
ABCB1what this gene does

ABCB1 is a gene that helps control how certain drugs are processed and cleared from a dog's body.

For your dog: If your dog is from a breed that carries this gene variant, ask your vet about medication sensitivities before giving any new drugs.

n = 4,815 dogs · 1 variant tested · OMIA:001503-9615 · omia.org →
ARSGwhat this gene does

ARSG is a gene that helps break down certain molecules in the body, keeping cells healthy.

For your dog: If your dog is from a breed known to carry ARSG mutations, it's worth discussing genetic testing with your vet to understand potential health risks.

n = 4,816 dogs · 2 variants tested · OMIA:000341-9615 · omia.org →
n = 4,816 dogs · 2 variants tested · OMIA:002120-9615 · omia.org →
NDRG1what this gene does

NDRG1 is a gene involved in nerve cell function and maintenance, helping keep the nervous system working properly.

For your dog: If your dog is from a breed known to carry NDRG1 variants, it’s worth discussing with your vet, especially if you notice any mobility issues.

Hypocatalasia
Autosomal recessive
low <0.1%
n = 4,815 dogs · 1 variant tested · OMIA:001138-9615 · omia.org →
CATwhat this gene does

CAT is a gene that helps produce an enzyme called catalase, which breaks down hydrogen peroxide in the body to prevent cell damage.

For your dog: If your dog is from a breed that can carry this gene, it’s worth asking your vet about testing. Being a carrier doesn’t mean your dog is affected, but it can inform health decisions.

Collie Eye Anomaly (CEA)
Autosomal recessive
low <0.1%
n = 4,816 dogs · 1 variant tested · OMIA:000218-9615 · omia.org →
NHEJ1what this gene does

NHEJ1 is a gene involved in repairing breaks in DNA, helping maintain the integrity of genetic information in cells.

For your dog: If your dog belongs to one of the breeds known to carry this gene variant, it's worth discussing testing with your vet to understand any potential eye health risks.

Shar-Pei Autoinflammatory Disease (SPAID)
Autosomal dominant (Incomplete penetrance)
low <0.1%
n = 4,816 dogs · 1 variant tested · OMIA:001561-9615 · omia.org →
MTBPwhat this gene does

MTBP is a gene involved in regulating inflammation in the body. It helps control how the immune system responds to triggers.

For your dog: If your dog is from a breed known to carry MTBP variants, it's worth discussing with your vet whether genetic testing or monitoring for inflammation-related issues makes sense.

Source: Donner J et al. 2023. Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs. PLOS Genetics 19(2):e1010651 · Evidence: Limited (DTC ascertainment, tag-SNP proxy) · Confounding MEDIUM · License CC-BY-4.0 · Phene IDs from OMIA (Sydney School of Veterinary Science, The University of Sydney; DOI 10.25910/2AMR-PV70).
Sample size in this breed: 4,816 dogs from the Donner 2023 cohort.
In plain terms

What these results mean for a Bulldog

39.4% of Bulldogs in the Donner 2023 cohort carried it (n=4,816).

  • The kidneys fail to reclaim an amino acid called cystine, which can form crystals and stones in the urine and block the urinary tract.
    OMIA 000256-9615

    “Cystinuria, type 1 - A is an inherited defect that causes failure of reabsorption of cystine in the proximal renal tubule, leading to cystine precipitation in the urine. Formation of crystals and calculi lead to urolithiasis and urinary tract obstruction.” OMIA 000256-9615

What to do
Straining to urinate, or passing little or no urine, needs a veterinarian the same day.

No test, or a mix
Without a test nobody can say how many copies a dog has.

12.7% of Bulldogs in the Donner 2023 cohort carried it (n=4,816).

  • DM is a loss of function in the spinal cord that begins in adulthood and progresses to paralysis of the back legs. There is no treatment that stops it.
    OMIA 000263-9615

    “This is an adult onset degeneration of the spinal cord that progresses to paraplegia and tetraparesis. There is no successful treatment. A genetic test is available.” OMIA 000263-9615

  • Two copies of the SOD1 variant mean at risk, not affected. Some dogs with two copies never show signs.
    OMIA 000263-9615

    “some homozygous mutant dogs had no signs of degenerative myelopathy, which suggests incomplete penetrance or other causative loci” OMIA 000263-9615

  • One copy makes a dog a carrier. In the study that found the variant, every affected dog tested had two copies.
    OMIA 000263-9615

    “All affected dogs tested were homozygous mutant.” OMIA 000263-9615

What to do
A DNA result is not a diagnosis. Take the result, and any change in how the dog walks, to a veterinarian.

No test, or a mix
Without a test nobody can say how many copies a dog has. A breed's carrier frequency describes the breed, not this dog.

55.5% of Bulldogs in the Donner 2023 cohort carried it (n=4,816).

  • The curated record finds no support for this variant causing cystinuria, and the researchers who studied it advise against using it as a test.
    OMIA 001880-9615

    “there appears to be no support for the variant to be causal” OMIA 001880-9615

    “strongly recommend not to use "the variant in SLC7A9 as a test to predict the risk of developing cystinuria in male English bulldogs.” OMIA 001880-9615

What to do
A carrier result for this variant does not predict bladder stones. Straining to urinate or blood in the urine is a reason to see a veterinarian whatever a DNA test says.

No test, or a mix
The curated record gives no reason to test for this variant.

Which Mendelian variants matter most for Bulldogs?

No Mendelian variants reached observable carrier frequency in the Bulldog cohort tested (Donner 2023). This is not the same as saying Bulldogs carry no recessive disease variants. It means the atlas sample (n=38) is too small to detect variants below roughly 10% carrier frequency, and the breed’s population bottleneck (genetic diversity rank 29 of 107) may have fixed some variants and purged others. The substrate cannot tell us which.

What we can see is the morphology. The breed standard calls for shortened limbs and a massive skull. That silhouette carries real health costs: airway restriction and heat intolerance are direct consequences. It sets the constraints for everything below: heat tolerance, breathing, joint loading, and lifespan.

What should I feed a Bulldog?

Bulldogs can’t pant efficiently, which means heat-of-the-day exercise is dangerous and meal timing matters more than it does for most breeds. Shortened limbs carry concentrated joint loading per stride. A Bulldog’s spine and hips are under constant mechanical stress that taller breeds distribute across longer bones.

Puppy feeding is where the joint trajectory gets set. A large-breed puppy formula with controlled calcium (0.8% to 1.2% on a dry-matter basis) and a calcium-to-phosphorus ratio between 1.1:1 and 2:1 is the foundation (NRC 2006). Bulldogs grow from 2 to 3 pounds at birth to 40 to 50 pounds at adulthood. That growth rate is fast enough that overfeeding calcium, even with a “large-breed” label, can accelerate joint disease. Feed to a growth chart, not to appetite. A Bulldog puppy should be lean enough that you feel the ribs without pressing.

Adult weight management is the other half. Bulldogs have a low spontaneous activity level compared to longer-limbed breeds, and owners often feed to the dog’s apparent appetite rather than to energy expenditure. Excess weight compounds the joint loading problem and is a documented concern in the breed (Bulldogclub.org health committee recommendations). Aim for a body condition score of 4 to 5 out of 9 (AAFCO standard). A calorie-controlled adult formula fed in measured portions, rather than free-feeding, is the generally accepted best practice for weight-prone brachycephalic breeds.

Heatstroke risk shifts meal timing. Bulldogs cannot thermoregulate efficiently, especially during exercise or in warm weather. Heavy meals during heat-of-the-day can impair panting and cooling. Feed the main meal in the cool morning and evening hours, with light treats only during midday. This is one of the few breed-specific feeding rules that is non-negotiable.

Grain-free diets carry unclear risk for this breed. The FDA’s 2018 advisory and Adin et al. 2019 (JVIM) flagged dilated cardiomyopathy in Goldens and some other breeds fed certain grain-free, pulse-heavy formulations. Bulldogs are not named in the FDA dataset with high frequency. The conservative default is still a grain-inclusive, taurine-supplemented adult formulation, but the evidence is less compelling for this breed than for Goldens or Dalmatians. Either approach is defensible; grain-inclusive is simply the safer assumption given the broader data.

What we don’t know

The atlas sample of 38 Bulldogs is below the threshold where Mendelian screening has statistical power. Carrier frequencies below roughly 10% will not surface, and the breed’s tight founder structure (24 dogs from Hayward 2016, 9 from Spatola, 3 from Jenkins, 1 from Shannon) means low-frequency recessives may be fixed or absent by chance rather than by health. We cannot say whether Bulldogs are truly free of recessive disease variants or whether the sample is simply too small to find them.

The breed’s shortened lifespan (atlas median 9.8 years (McMillan 2024 / VetCompass)) is consistent with the severe morphology, shortened limbs, compact skull, flat face, and small nasal passages. We do not know how much of the lifespan gap is unavoidable given the breed standard and how much is modifiable through selection, weight management, and early intervention for airway obstruction and heat intolerance. The honest summary is that the breed’s conformation sets hard limits that we have not yet parsed from modifiable risk.

Frequently asked questions about Bulldogs

Why do Bulldogs have such short lifespans? The atlas median is 9.8 years (McMillan 2024 / VetCompass) (Donner 2023), well below the all-breed median. The shortened limbs, compact skull, and flat face that define the breed standard also constrain heat tolerance, airway capacity, and joint geometry. These are the breed, not fixable through diet alone.

Are Bulldogs prone to hip dysplasia? Yes. The breed’s low back-to-hip ratio and concentrated joint loading create a geometric predisposition. The OFA has not published a breed-specific prevalence figure for Bulldogs. Weight management and controlled growth in puppyhood are the primary preventions.

Can I overfeed a Bulldog puppy? Yes, and it matters. Overfeeding calcium and calories in large-breed puppies accelerates joint disease. Use a large-breed puppy formula and feed to a growth chart, not to appetite. A lean puppy at 12 weeks will thank you at age five.

Should I feed my Bulldog grain-free? Not unless your vet identifies a specific protein allergy. The FDA’s cardiac-risk advisory did not flag Bulldogs as a primary-affected breed, but grain-inclusive formulations remain the conservative default. Ensure the food is taurine-supplemented either way.

What time of day should I feed my Bulldog? Early morning and evening, when it is cool. Bulldogs can’t pant efficiently, and digestion during heat-of-the-day can impair cooling. This is non-negotiable in summer and warm climates.

Is my Bulldog’s breathing normal? Not necessarily. Many Bulldogs have airway obstruction (brachycephalic obstructive airway syndrome, BOAS) that owners interpret as normal snoring. If your Bulldog struggles to cool down after light exercise, has noisy breathing at rest, or seems to tire quickly, ask your vet about airway assessment. Early surgical intervention for BOAS is associated with improved respiratory function in affected dogs (Poncet et al. 2006, JSAP 47:315-323).

Do Bulldogs need special joint supplements? Peer-reviewed evidence supporting glucosamine or chondroitin as prevention for hip dysplasia is lacking across breeds (Innes et al. 2003, JSAP 44:400). Weight management and controlled growth are proven. Supplements are an optional add-on, not a substitute.

Should I get a DNA test for my Bulldog? A whole-genome sequence would be informative (the atlas has only 38 dogs), but a commercial panel would not flag Mendelian variants at the carrier frequency in the current substrate. If you breed, a sequence is worth considering for future population management. For a pet, it is optional.

Names & origins

Other names

The Bulldog is also recorded as British Bulldog and English Bulldog.

Identified as Bulldog (VBO:0200258) in the Vertebrate Breed Ontology (Mullen et al. 2025, CC-BY 4.0) · registry IDs FCI 149 · iDog 58 · VeNom 13759.

For researchers Population genetics, disease models and every recorded condition Open the research detail for the Bulldog
What the atlas says about Bulldog

In the atlas, the Bulldog clusters consistently as Bulldog (100% of the 38 dogs here). Dogs here sit in a relatively sparse region of the atlas, fewer close neighbors than typical.

Median lifespan is 8.6 years, about 3.2 years shorter than a typical dog of 24.0 kg, one of the larger gaps in the atlas.

Genetic dimensions · CanVAS atlas

What the atlas genotypes say about Bulldog

Computed from the 14,478 CanVAS dogs in the Atlas, on an imputed genotype backbone: 77,215 directly typed sites per dog, imputed to 9.67 million variants.

The confidence below counts dogs, not reads: it is the size of the sample, and it is separate from how the genotypes were measured.

Dogs in the Atlas
38Founders
24 from Hayward2016, 9 from Spatola, 3 from JenkinsWGS
Genetic diversity
0.29Moderate
Mean heterozygosity across the breed. 79th most diverse of 107 ranked populations.
What does genetic diversity mean?

How varied a breed's gene pool is — the share of gene spots where a typical dog of the breed carries two different versions rather than two identical ones.

How to read it: Higher = more diverse. Among well-sampled breeds it ranges roughly 0.22 (least diverse) to 0.33 (most diverse).

Diversity is a strength, not a verdict on any individual dog. Lower diversity means it's worth paying attention to recessive-risk testing — not that a dog is doomed.

Cluster structure
Splits into two genetic sub-populations
Intra-breed RMS distance: 49.88 · likely working/show-line, regional, or kennel lineage split.
What does within-breed variation mean?

How much individual dogs within the breed differ from each other genetically.

How to read it: Higher = more internal variety among individuals of the breed.

Sensitive to how many dogs of the breed we've sampled.

Related breeds
Gave rise to
In the Non-Sporting group
Explore the full lineage map →
VBO foundation stock (breeding records) · AKC breed group
Relatedness is documented lineage + kennel family. Genetic-ancestry distance measures diversity, not kinship, so it isn't used here.
How long they live
9.8years (life expectancy)
95% CI 9.7–10 · VetCompass, McMillan 2024, n=11,065. source
What does typical lifespan mean?

The median age dogs of the breed tend to reach.

How to read it: Higher = longer-lived. Compare to longevity-for-size to see whether it's just a size effect.

Drawn from population lifespan records; individual dogs vary widely with care, genetics, and luck.

n = 38 dogs · moderate sample · CanVAS (Brundage 2026) · Sniff Atlas
A gift to human medicine

Bulldogs are a natural model for human disease

Because the same genes cause the same conditions across species, the inherited conditions documented in Bulldogs help researchers understand, and work toward treating, the human diseases they model. This is the dog advancing human medicine. The breed models the human disease; it does not have it, and this is not a prediction for your dog.

Human equivalents via OMIA → Mondo / OMIM. Model-of, not identity. The named gene is the canine locus, not a claim that a pet has the human disease.
Documented in OMIA

Every condition recorded in the Bulldog

Beyond the testable carriers above, OMIA's literature catalogue records 4 genetic conditions in the Bulldog, 3 of which have a known human equivalent. This is the documented landscape across all Bulldogs ever studied, not a prediction for any one dog.

Online Mendelian Inheritance in Animals (OMIA); Nicholas, Tammen & Sydney Informatics Hub, DOI 10.25910/2AMR-PV70
Documented in the breed's literature is not carrier status and not a forecast for an individual dog. Human equivalents are mapped via Mondo/OMIM. Carrier frequencies (above) are the separately-measured testable subset (Donner 2023).
The data behind this page

Where every number on this page came from.

This page draws on three primary data sources. Carrier frequencies for the Mendelian section come from Donner et al. 2023 (CC-BY-4.0). We grade these data at evidence Limited because the cohort is a direct-to-consumer ascertainment, which biases toward owners who chose to test their dogs. The panel also uses tag-SNP proxies for some variants rather than direct causal-variant assays. Limited is a study-design grade, not a quality grade: the Donner cohort is the largest open canine-genotype dataset in existence and we are grateful for it. We rate the confounding MEDIUM.

Population-genetic dimensions (heterozygosity, intra-breed PCA distance, nearest neighbors, trait-locus frequencies) come from CanVAS (Brundage 2026), harmonized through the Sniff Atlas. The exact release date and verification commit are pinned at the bottom of the page so a researcher can trace a number back to a specific snapshot. The disease-gene-variant graph comes from OMIA (Online Mendelian Inheritance in Animals; Nicholas, Tammen, and the Sydney Informatics Hub at the Sydney School of Veterinary Science, The University of Sydney; retrieved April 2026, DOI 10.25910/2AMR-PV70).

What this page does not yet have. Inheritance modes and per-disease penetrance evidence from Donner 2023 are in the structured data for every variant the panel covers. Mondo, OMIM, Ensembl, and HGNC cross-references live on the gene and disease pages this page links to, rather than being repeated here. What is still absent from this breed page is anything not in the cited panel, and each such gap carries its cause where it appears.

How to cite this page. The computed dimensions on this page are derived from the open Sniff Atlas v1.0.1 (Gehring 2026, doi:10.5281/zenodo.20566358, CC-BY 4.0). Full citation formats including BibTeX, RIS, and CITATION.cff at sniff.world/cite.

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References
  1. Donner J, Freyer J, Davison S, Anderson H, Blades M, Honkanen L, et al. (2023). Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs. PLOS Genetics 19(2):e1010651. doi:10.1371/journal.pgen.1010651
  2. Brundage DM (2026). CanVAS: A Harmonized and Imputed Canine Variant Atlas. bioRxiv. doi:10.64898/2026.04.13.718238
  3. Nicholas, F.W., Tammen, I., & Sydney Informatics Hub. (2026). Online Mendelian Inheritance in Animals (OMIA) [dataset]. The University of Sydney. https://omia.org. doi:10.25910/2AMR-PV70 (retrieved April 2026).
Last updated
Sources: CanVAS (Brundage 2026) · Donner 2023 · OMIA