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English Toy Spaniel Detail Information
General Information

iDog Breed Number: CB98
Original: England
Personality:
Energy Level: Somewhat Active; Cavorting and curious at play; well-behaved and dignified at home
Good With Children: Yes
Good with other Dogs: Yes
Shedding: Seasonal
Grooming: Weekly
Trainability: Responds Well
Height: 22.9-25.4 cm
Weight: 3.6-6.4 kg
Life Expectancy: 10-12 years
Barking Level: Quiet
History:


Web Source Name: English Toy Spaniel from AKC
Other Name: King Charles Spaniel; Toy Spaniel; Charlies; Prince Charles Spaniel; Ruby Spaniel; Blenheim Spaniel

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
Allergies      OMIM: 9123
Anasarca      OMIM: 9123
Apocrine gland tumor      OMIM: 9123
Basal cell tumor      OMIM: 9123
Behavioral abnormalities      OMIM: 9123
Cataract with microphthalmia      OMIM: 9123
Cleft palate DLX6  OMIA:      OMIM: 9123
Coloboma      OMIM: 9123
Cranioschisis      OMIM: 9123
Distichiasis      OMIM: 9123
Epidermoid cyst      OMIM: 9123
Epilepsy LGI2  DIRAS1  OMIA:      OMIM: 9123
Factor X deficiency      OMIM: 9123
Factor XI deficiency F11  OMIA:      OMIM: 9123
Hemolytic anemia      OMIM: 9123
Inguinal hernia      OMIM: 9123
Lip fold dermatitis      OMIM: 9123
Melanoma      OMIM: 9123
Osteochondritis dissecans      OMIM: 9123
Otitis externa      OMIM: 9123
Overshot jaw      OMIM: 9123
Renal cortical hypoplasia      OMIM: 9123
Sebaceous gland tumor      OMIM: 9123
Skin neoplasms      OMIM: 9123
Narcolepsy HCRTR2  OMIA:      OMIM: 9123
Osteochondrosis      OMIM: 9123
Rage syndrome      OMIM: 9123
Ehlers Danlos syndrome      OMIM: 9123
Cataract HSF4  have an increased incidence OMIA:      OMIM: 9123
Cleft lip ADAMTS20  may be inherited OMIA:      OMIM: 9123
Corneal dystrophy LOC489707  may be inherited OMIA:      OMIM: 9123
Cutaneous asthenia      OMIM: 9123
Ectropion      OMIM: 9123
Elbow dysplasia      OMIM: 9123
Entropion      OMIM: 9123
Glaucoma ADAMTS10  NEB  ADAMTS17  OMIA:      OMIM: 9123
Hemophilia A F8  OMIA:      OMIM: 9123
Hemophilia B F9  OMIA:      OMIM: 9123
Hip dysplasia      OMIM: 9123
Hydrocephalus      OMIM: 9123
Hypomyelinogenesis      OMIM: 9123
Addison's disease (hypoadrenocorticism)      OMIM: 9123
Hypothyroidism TPO  OMIA:      OMIM: 9123
Intervertebral disc disease FGF4 retrogene in CFA12  OMIA:      OMIM: 9123
Lysosomal storage diseases      OMIM: 9123
Optic nerve hypoplasia      OMIM: 9123
Patella luxation      OMIM: 9123
Patent ductus arteriosus      OMIM: 9123
Persistent pupillary membrane      OMIM: 9123
Phosphofructokinase deficiency      OMIM: 9123
Progressive retinal atrophy (Rod-cone dysplasia) CNGB1  RPGR  GNGT2  PDE6B  RD3  PDE6A  C17H2orf71  SAG  FAM161A  MERTK  CNGA1  OMIA:      OMIM: 9123
Retinal dysplasia have an increased incidence      OMIM: 9123
Seborrhea      OMIM: 9123
Associated SNP Information
There are no associated SNPs
Breed Standards
Reference
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