French Bulldog
Bouledogue Francais, Fransk Bulldogg, Bulldog Francés, Französiche Bulldogge, Ranskanbulldoggi
French Bulldog
FCI Group
Companion and Toy Dogs
AKC Group
Non-Sporting
TKC Group
Utility
Country of Origin
FR
French Bulldog
Health Testing Requirements by Country
Autoimmune and Allergies
FI
Cardiac and Circulatory
Ataxia, Locomotor, and Epilepsy
Eye Conditions and Blindness
US
Gastrointestinal, Digestive, and Metabolic
Skeletal and Muscular
Neurological and Neuromuscular
Cancer and Neoplasia
Reproductive
Respiratory
Skin, Hair, and Nails
UK
Temperament
Other Breed-Specific Considerations
Other Genetic Testing
Test Relevances
Hyperuricosuria and Hyperuricemia (HUU)
Moderate Relevance
Respiratory Function Grading Scheme (RFGS)
Moderate Relevance
Primary Hereditary Cataract (PHC)
Some Relevance
Screw tail
Some Relevance
Respiratory Function Grading Scheme (RFGS)
Some Relevance
Chondrodystrophy (CDDY and IVDD)
Some Relevance
Congenital Hypothyroidism
Some Relevance
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
No Evidence
Canine Multifocal Retinopathy 1 (cmr1)
No Evidence
Coat Colour Dilution, dilution, MLPH-related
No Evidence
Cystinuria Type I-A
No Evidence
Cystinuria Type II-A
No Evidence
Cystinuria Type II-B
No Evidence
Degenerative Myelopathy
Inconclusive
Chondrodysplasia (CDPA)
Not Recommended
Hyperuricosuria and Hyperuricemia (HUU)
Moderate Relevance
Respiratory Function Grading Scheme (RFGS)
Moderate Relevance
Primary Hereditary Cataract (PHC)
Some Relevance
Screw tail
Some Relevance
Research suggests that this variant is associated with many clinical symptoms associated with brachycephalic conformation associated conditions. Variant may be fixed in some breeds.
Respiratory Function Grading Scheme (RFGS)
Some Relevance
Chondrodystrophy (CDDY and IVDD)
Some Relevance
Congenital Hypothyroidism
Some Relevance
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
No Evidence
Reported only in miniature long-haired dachshunds (and their crosses).
Canine Multifocal Retinopathy 1 (cmr1)
No Evidence
Currently no breed-specific reference found, but multiple references in closely related breeds indicating may be relevant to this breed.
Coat Colour Dilution, dilution, MLPH-related
No Evidence
Cystinuria Type I-A
No Evidence
Possibly incorrect mutation for this breed. See cystinuria type II-A
Cystinuria Type II-A
No Evidence
Cystinuria Type II-B
No Evidence
Degenerative Myelopathy
Inconclusive
Both clinically rare and of complex inheritance. Test is considered poorly correlated with risk for development of DM, and recommendations are to not use the test for breed-wide breeding strategies. While the SOD 1 variant may be commonly found across many breeds, there are few clinical cases observed and confirmed, and in many cases DM has never been observed in the breeds.
Chondrodysplasia (CDPA)
Not Recommended
Connections
- Updated