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Pembroke Welsh Corgi Detail Information
General Information

iDog Breed Number: CB179
Original: United Kingdom(Wales)
Personality:
Energy Level: Very Active; A strong and athletic little dog, the Pembroke loves physical activity and is happiest when he has a job to do.
Good With Children: Better with Supervision
Good with other Dogs: With Supervision
Shedding: Frequent
Grooming: Occasional
Trainability: Responds Well
Height: 25.4-30.5 cm
Weight: up to 13.6 kg (male), up to 12.7 kg (female)
Life Expectancy: 12-13 years
Barking Level: Barks When Necessary
History:


Web Source Name: Pembroke Welsh Corgi from AKC
Common Name: Pembroke; PWC; Pem; Corgi; Welsh Corgi

Breed Registries
AKC
CKC
UKC
FCI
Yes
 Yes
 Yes
 No
Associated Disease Information
Disease Name Gene Name Disease Level (CIDD) Associated Links
Distichiasis      OMIM: 9123
Hemolytic anemia      OMIM: 9123
Hypoplasia of dens      OMIM: 9123
Inguinal hernia      OMIM: 9123
Keratitis sicca      OMIM: 9123
Pigmentary keratitis      OMIM: 9123
Sertoli cell tumor      OMIM: 9123
Short skull      OMIM: 9123
Swimmer puppies      OMIM: 9123
Ulcerative keratitis      OMIM: 9123
Umbilical hernia      OMIM: 9123
Thrombocytopenia TUBB1  OMIA:      OMIM: 9123
Cataract HSF4  have an increased incidence OMIA:      OMIM: 9123
Corneal dystrophy LOC489707  have an increased incidence OMIA:      OMIM: 9123
Cutaneous asthenia have an increased incidence      OMIM: 9123
Myelopathy SOD1  SP110  have an increased incidence OMIA:      OMIM: 9123
Dermatomyositis may be inherited      OMIM: 9123
Entropion      OMIM: 9123
Familial kidney disease have an increased incidence      OMIM: 9123
Facial fold dermatitis      OMIM: 9123
Hypothyroidism TPO  OMIA:      OMIM: 9123
Idiopathic epilepsy may be inherited      OMIM: 9123
Lacrimal duct atresia      OMIM: 9123
Intervertebral disc disease FGF4 retrogene in CFA12  have an increased incidence OMIA:      OMIM: 9123
Keratoconjunctivitis sicca FAM83H  OMIA:      OMIM: 9123
Lens luxation ADAMTS17  OMIA:      OMIM: 9123
Microphthalmia      OMIM: 9123
Pannus      OMIM: 9123
Persistent pupillary membrane have an increased incidence      OMIM: 9123
Progressive retinal atrophy (Rod-cone dysplasia) CNGB1  RPGR  GNGT2  PDE6B  RD3  PDE6A  C17H2orf71  SAG  FAM161A  MERTK  CNGA1  may be inherited OMIA:      OMIM: 9123
Retinal dysplasia have an increased incidence      OMIM: 9123
von Willebrand's disease VWF  have an increased incidence OMIA:      OMIM: 9123
Associated SNP Information
There are no associated SNPs
Breed Standards
Reference
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