Cocker Spaniel Detail Information
General Information

iDog Breed Number: CB78
Personality:
Energy Level: Very Active; Energetic sporting dogs, Cockers love their playtime and brisk walks
Good With Children: Yes
Good with other Dogs: Yes
Shedding: Seasonal
Grooming: Weekly
Trainability: Eager To Please
Height: 36.8-39.4 cm (male), 34.3-36.8 cm (female)
Weight: 11.3-13.6 kg (male), 9.1-11.3 kg (female)
Life Expectancy: 10-14 years
Barking Level: Barks When Necessary
History:


Web Source Name: Cocker Spaniel from AKC
Other Name: American Cocker Spaniel (American breed outside of America), English Cocker Spaniel (British breed, outside of Britain)
Common Name: Cockers

Breed Registries
AKC
CKC
UKC
FCI
Yes
No Yes
No
Associated Disease Information
Disease Name Gene Name Disease Level (CIDD) Associated Links
Aberrant cilia      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
Cranioschisis      OMIM: 9123
Cyclic neutropenia AP3B1  OMIA:      OMIM: 9123
Distichiasis      OMIM: 9123
Epidermoid cyst      OMIM: 9123
Epilepsy LGI2  DIRAS1  OMIA:      OMIM: 9123
Factor X deficiency      OMIM: 9123
Hemolytic anemia      OMIM: 9123
Inguinal hernia      OMIM: 9123
Keratitis sicca      OMIM: 9123
Lip fold dermatitis      OMIM: 9123
Melanoma      OMIM: 9123
Osteochondritis dissecans      OMIM: 9123
Otitis externa      OMIM: 9123
Overshot jaw      OMIM: 9123
Perianal gland tumor      OMIM: 9123
Primary peripheral retinal dystrophy      OMIM: 9123
Renal cortical hypoplasia      OMIM: 9123
Skin neoplasms      OMIM: 9123
Tail abnormalities      OMIM: 9123
Teeth abnormalities      OMIM: 9123
Umbilical hernia      OMIM: 9123
Undershot jaw      OMIM: 9123
Ununited anconeal process      OMIM: 9123
Primary uterine inertia      OMIM: 9123
Osteochondrosis      OMIM: 9123
Ehlers Danlos syndrome      OMIM: 9123
Atopy have an increased incidence      OMIM: 9123
Cataract HSF4  have an increased incidence OMIA:      OMIM: 9123
Chronic hepatitis have an increased incidence      OMIM: 9123
Cleft lip ADAMTS20  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
Cutaneous asthenia      OMIM: 9123
Dilated cardiomyopathy may be inherited      OMIM: 9123
Disorders of sexual development - sexual reversal HSD17B3  have an increased incidence OMIA:      OMIM: 9123
Ectropion      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
Hemophilia B F9  OMIA:      OMIM: 9123
Hip dysplasia have an increased incidence      OMIM: 9123
Hydrocephalus      OMIM: 9123
Hypothyroidism TPO  have an increased incidence OMIA:      OMIM: 9123
Idiopathic epilepsy have an increased incidence      OMIM: 9123
Immune-mediated hemolytic anemia (IMHA) have an increased incidence      OMIM: 9123
Immune-mediated thrombocytopenia have an increased incidence      OMIM: 9123
Intervertebral disc disease FGF4 retrogene in CFA12  may be inherited OMIA:      OMIM: 9123
Keratoconjunctivitis sicca FAM83H  have an increased incidence OMIA:      OMIM: 9123
Lens luxation ADAMTS17  OMIA:      OMIM: 9123
Lysosomal storage diseases      OMIM: 9123
Patella luxation may be inherited      OMIM: 9123
Patent ductus arteriosus have an increased incidence      OMIM: 9123
Persistent pupillary membrane have an increased incidence      OMIM: 9123
Phosphofructokinase deficiency have an increased incidence      OMIM: 9123
Platelet disorder have an increased incidence      OMIM: 9123
Portosystemic shunt may be inherited      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
Pulmonic stenosis have an increased incidence      OMIM: 9123
Retinal dysplasia Most Important      OMIM: 9123
Sebaceous adenitis have an increased incidence      OMIM: 9123
Seborrhea Most Important      OMIM: 9123
Sick sinus syndrome have an increased incidence      OMIM: 9123
Eversion of nictitating membrane have an increased incidence      OMIM: 9123
vitamin A-responsive dermatosis have an increased incidence      OMIM: 9123
von Willebrand's disease VWF  OMIA:      OMIM: 9123
Associated SNP Information
There are no associated SNPs