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Gordon Setter Detail Information
General Information

iDog Breed Number: CB117
Original: United Kingdom (Scotland)
Personality:
Energy Level: Somewhat Active; Athletic and outdoorsy, Gordons need activity to stave off boredom
Good With Children: Better with Supervision
Good with other Dogs: With Supervision
Shedding: Seasonal
Grooming: Occasional
Trainability: Responds Well
Height: 61-68.6 cm (male), 58.4-66 cm (female)
Weight: 24.9-36.3 kg (male), 20.4-31.8 kg (female)
Life Expectancy: 12-13 years
Barking Level: Likes To Be Vocal
History:


Web Source Name: Gordon Setter from AKC

Breed Registries
AKC
CKC
UKC
FCI
Yes
 Yes
 Yes
 Yes
Associated Disease Information
Disease Name Gene Name Disease Level (CIDD) Associated Links
Acute moist dermatitis      OMIM: 9123
Allergies      OMIM: 9123
Coloboma      OMIM: 9123
Atopic dermatitis      OMIM: 9123
Distichiasis      OMIM: 9123
Folliculitis      OMIM: 9123
Furunculosis      OMIM: 9123
Granulomatous sebaceous adenitis      OMIM: 9123
Hemolytic anemia      OMIM: 9123
Hepatic portosystemic shunt      OMIM: 9123
Juvenile cellulitis      OMIM: 9123
Lymphocytic thyroiditis      OMIM: 9123
Lymphosarcoma      OMIM: 9123
Osteochondritis dissecans      OMIM: 9123
Thyroiditis      OMIM: 9123
Vogt-Koyanagi-Harada-like syndrome      OMIM: 9123
Fragmented coronoid process      OMIM: 9123
Hemangiosarcoma      OMIM: 9123
Muscular dystrophy DMD  COL6A1  SGCD  OMIA:      OMIM: 9123
Osteochondrosis      OMIM: 9123
Acral lick dermatitis      OMIM: 9123
Atopy      OMIM: 9123
Cataract HSF4  have an increased incidence OMIA:      OMIM: 9123
Cerebellar cortical abiotrophy have an increased incidence      OMIM: 9123
Corneal dystrophy LOC489707  OMIA:      OMIM: 9123
Ectropion      OMIM: 9123
Elbow dysplasia      OMIM: 9123
Entropion      OMIM: 9123
Follicular dysplasias have an increased incidence      OMIM: 9123
Gastric dilatation-volvulus have an increased incidence      OMIM: 9123
Hemophilia A F8  OMIA:      OMIM: 9123
Hip dysplasia Most Important      OMIM: 9123
Hypothyroidism TPO  OMIA:      OMIM: 9123
Keratoconjunctivitis sicca FAM83H  may be inherited OMIA:      OMIM: 9123
Myasthenia gravis      OMIM: 9123
Optic nerve hypoplasia      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
Retinal dysplasia have an increased incidence      OMIM: 9123
Sebaceous adenitis      OMIM: 9123
Subaortic stenosis      OMIM: 9123
Vitiligo      OMIM: 9123
Associated SNP Information
There are no associated SNPs
Breed Standards
Reference
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