English Springer Spaniel Detail Information
General Information

iDog Breed Number: CB97
Original: United Kingdom (England)
Personality:
Energy Level: Very Active; Built for long days as hunters’ companions, Springers need regular exercise for optimum mental and physical health
Good With Children: Better with Supervision
Good with other Dogs: With Supervision
Shedding: Seasonal
Grooming: Occasional
Trainability: Eager To Please
Height: 50.8 cm (male), 48.3 cm (female)
Weight: 22.7 kg (male), 18.1 kg (female)
Life Expectancy: 12-14 years
Barking Level: Barks When Necessary
History:


Web Source Name: English Springer Spaniel from AKC
Other Name: Springer Spaniel

Breed Registries
AKC
CKC
UKC
FCI
Yes
Yes
Yes
Yes
Associated Disease Information
Disease Name Gene Name Disease Level (CIDD) Associated Links
Bloat      OMIM: 9123
Color mutant alopecia MLPH  OMIA:      OMIM: 9123
Eclampsia      OMIM: 9123
Hypoglycemia      OMIM: 9123
Juvenile amaurotic idiocy      OMIM: 9123
Neuronal ceroid lipofuscinosis CLN6  TPP1  CLN5  ARSG  PPT1  CTSD  CLN8  ATP13A2  MFSD8  OMIA:      OMIM: 9123
Osteochondritis dissecans      OMIM: 9123
Uterine eclampsia      OMIM: 9123
Familial amaurotic idiocy      OMIM: 9123
Lipidosis      OMIM: 9123
Osteochondrosis      OMIM: 9123
Cataract HSF4  have an increased incidence OMIA:      OMIM: 9123
Coagulation (bleeding) disorders P2RY12  have an increased incidence OMIA:      OMIM: 9123
Corneal dystrophy LOC489707  have an increased incidence OMIA:      OMIM: 9123
Craniomandibular osteopathy      OMIM: 9123
Cutaneous asthenia have an increased incidence      OMIM: 9123
Deafness      OMIM: 9123
Diabetes mellitus have an increased incidence      OMIM: 9123
Ectropion have an increased incidence      OMIM: 9123
Entropion have an increased incidence      OMIM: 9123
Facial fold dermatitis have an increased incidence      OMIM: 9123
Glaucoma ADAMTS10  NEB  ADAMTS17  may be inherited OMIA:      OMIM: 9123
Hemophilia A F8  OMIA:      OMIM: 9123
Hip dysplasia Most Important      OMIM: 9123
Hypomyelinogenesis have an increased incidence      OMIM: 9123
Hypothyroidism TPO  OMIA:      OMIM: 9123
Idiopathic epilepsy may be inherited      OMIM: 9123
Immune-mediated hemolytic anemia (IMHA) have an increased incidence      OMIM: 9123
Keratoconjunctivitis sicca FAM83H  OMIA:      OMIM: 9123
Lysosomal storage diseases have an increased incidence      OMIM: 9123
Myasthenia gravis have an increased incidence      OMIM: 9123
Patent ductus arteriosus have an increased incidence      OMIM: 9123
Phosphofructokinase deficiency Most Important      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
Progressive retinal atrophy (Rod-cone dysplasia) CNGB1  RPGR  GNGT2  PDE6B  RD3  PDE6A  C17H2orf71  SAG  FAM161A  MERTK  CNGA1  have an increased incidence OMIA:      OMIM: 9123
psoriasiform-lichenoid dermatosis have an increased incidence      OMIM: 9123
Retinal dysplasia Most Important      OMIM: 9123
Seborrhea Most Important      OMIM: 9123
Ventricular septal defect may be inherited      OMIM: 9123
von Willebrand's disease VWF  OMIA:      OMIM: 9123
Associated SNP Information
There are no associated SNPs