French Bulldog: inherited diseases and health

Updated 2026-09-30 · 3 sources

Based on: OMIA (University of Sydney), Science for Animal Welfare (UFAW), Wikidata

Breed health

The inherited conditions below have been documented in this breed in published research. That does not mean your dog has them or will get them – but it helps to know the names when you talk to a breeder or a vet.

Conditions this breed is prone to

Veterinary charities list this breed as more likely than others to get these conditions. Read the signs and what to do:

French Bulldog and chocolate: how much is dangerous?

Typical adult weight: 8–14 kg. Grams of chocolate at which signs can start (20 mg/kg) and at which severe signs are reported (40 mg/kg):

Dog weightMilkDark 70–85%Baking / unsweetened
8 kg80 g signs
160 g severe
20 g signs
40 g severe
11 g signs
23 g severe
14 kg140 g signs
280 g severe
35 g signs
70 g severe
20 g signs
40 g severe

Based on published doses: signs from about 20 mg/kg, severe signs from 40 mg/kg (US FDA, Cortinovis & Caloni 2016, Swedish Poison Information Centre). An estimate, not a diagnosis.

Check the exact amount with the chocolate calculator →

Inherited conditions documented in the breed

Conditions documented: 25

A gene variant is known for 12 of the conditions below, so a DNA test may exist. Ask your vet or the breed club.

ConditionBody systemInheritanceGene variant known
Alexander disease[1]Nervous systemAutosomal dominantYes
Brachycephalic Airway Obstruction Syndrome (BAOS)[2]–––
Cataract, early onset, HSF4-related[1]Vision / eyeAutosomal recessiveYes
Coat colour, merle[1]PigmentationAutosomal incomplete dominantYes
Complex vertebral malformation[1]Skeleton (incl. short stature & teeth)––
Cystinuria, type I - A[1]Renal / urinary systemAutosomal recessiveYes
Degenerative myelopathy[1]Nervous systemAutosomal recessiveYes
Dermoid sinus[1]Integument (skin)–Yes
Eyelid gland, third, prolapse of[1]Vision / eye–No
Haemophilia B[1]Haematopoietic systemX-linked recessiveYes
Hemivertebrae[2]–––
Hydrops foetalis[1]Embryo––
Hypothyroidism, congenital[1]Endocrine / exocrine gland (incl mammary gland)Autosomal recessiveYes
Inflammatory bowel disease[1]Digestive / alimentary––
Intervertebral disc disease, predisposition to[1]Skeleton (incl. short stature & teeth)Autosomal dominantYes
Meningoencephalitis[1]Nervous systemMultifactorialNo
Muscle hypertrophy, dysphagia, and gait abnormalities[1]Nervous system––
Myoclonus epilepsy of Lafora[1]Behaviour / neurologicalAutosomal recessiveYes
Myotonia[1]MuscleAutosomal recessiveYes
Pulmonary valve dysplasia[1]Cardiovascular systemMultifactorialNo
Screw tail[1]Limbs / fins / digit / tailAutosomal recessiveYes
Spinal intradural arachnoid diverticulum[1]Nervous system––
Syringomyelia[1]Nervous systemMultifactorialNo
Tetragametic chimerism (including Freemartin)[1]Reproductive system–No
XX difference of sexual development, generic[1]Reproductive systemMultifactorialNo

What this list means

  • “Documented in the breed” means at least one published case or study – it says nothing about how common the condition is.
  • Many of these conditions are rare. A responsible breeder can tell you which health tests the parents have had.
  • Where the gene variant is known, a DNA test may exist – ask your vet or the breed club.
  • If your pet shows signs of illness, contact your vet. This page cannot tell you whether your pet is ill.

About the breed

Origin
France
Height
24–35 cm
Weight
8–14 kg
FCI number
101
[3]
If your pet is struggling to breathe, has collapsed, is having a seizure or can't stand up: go to the nearest vet now.

Not sure how serious it is?

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Sources

  1. OMIA (University of Sydney)
  2. Science for Animal Welfare (UFAW)
  3. Wikidata

How this page was made: the list is taken directly from the sources below; nothing on it was written by AI. Names of conditions may be machine-translated. It is information, not a diagnosis. How we write our pages

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