Welsh Springer Spaniel Detail Information
General Information

iDog Breed Number: CB253
Original: United Kingdom (Wales)
Personality:
Energy Level: Very Active; Curious and highly energetic, Welshies need regular exercise to stave off problem behaviors
Good With Children: Yes
Good with other Dogs: With Supervision
Shedding: Seasonal
Grooming: Occasional
Trainability: Eager To Please
Height: 45.7-48.3 cm (male), 43.2-45.7 cm (female)
Weight: 18.1-24.9 kg (male), 15.9-22.7 kg (female)
Life Expectancy: 12-15 years
Barking Level: Barks When Necessary
History:


Web Source Name: Welsh Springer Spaniel from AKC
Other Name: Welsh Springer;Welsh Cocker Spaniel;Welsh Starter
Common Name: Welshie

Breed Registries
AKC
CKC
UKC
FCI
Yes
Yes
Yes
Yes
Associated Disease Information
Disease Name Gene Name Disease Level (CIDD) Associated Links
Abnormal copper metabolism      OMIM: 9123
Bloat      OMIM: 9123
Color mutant alopecia MLPH  OMIA:      OMIM: 9123
Distichiasis      OMIM: 9123
Eosinophilic panosteitis      OMIM: 9123
Gastric torsion      OMIM: 9123
Granulomatous sebaceous adenitis      OMIM: 9123
Hairlessness      OMIM: 9123
Hypertrophic osteodystrophy      OMIM: 9123
Hyposomatotropism      OMIM: 9123
Immunoglobulin G deficiency      OMIM: 9123
Immunoglobulin M deficiency      OMIM: 9123
Mastocytoma      OMIM: 9123
Syringomyelia      OMIM: 9123
Umbilical hernia      OMIM: 9123
Undershot jaw      OMIM: 9123
Vasculitis      OMIM: 9123
Thymic atrophy      OMIM: 9123
Cell-mediated immunodeficiency      OMIM: 9123
Cataract HSF4  have an increased incidence OMIA:      OMIM: 9123
Corneal dystrophy LOC489707  OMIA:      OMIM: 9123
Elbow dysplasia      OMIM: 9123
Entropion      OMIM: 9123
Glaucoma ADAMTS10  NEB  ADAMTS17  have an increased incidence OMIA:      OMIM: 9123
Hemophilia A F8  OMIA:      OMIM: 9123
Hip dysplasia Most Important      OMIM: 9123
Hypomyelinogenesis      OMIM: 9123
Hypothyroidism TPO  may be inherited OMIA:      OMIM: 9123
Myasthenia gravis      OMIM: 9123
Spinal dysraphism NKX2-8  OMIA:      OMIM: 9123
Progressive retinal atrophy (Rod-cone dysplasia) CNGB1  RPGR  GNGT2  PDE6B  RD3  PDE6A  C17H2orf71  SAG  FAM161A  MERTK  CNGA1  have an increased incidence OMIA:      OMIM: 9123
Sebaceous adenitis      OMIM: 9123
Immunoglobulin A deficiency      OMIM: 9123
Eversion of nictitating membrane      OMIM: 9123
Associated SNP Information
There are no associated SNPs