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German Short-Haired Pointer Detail Information
General Information

iDog Breed Number: CB111
Original: Germany
Personality:
Energy Level: Very Active; Like most pointing breeds, GSPs thrive on running and exercise
Good With Children: Yes
Good with other Dogs: With Supervision
Shedding: Seasonal
Grooming: Occasional
Trainability: Eager To Please
Height: 58.4-63.5 cm (male), 53.3-58.4 cm (female)
Weight: 24.9-31.8 kg (male), 20.4-27.2 kg (female)
Life Expectancy: 10-12 years
Barking Level: Barks When Necessary
History:


Web Source Name: German Shorthaired Pointer from AKC
Other Name: Deutscher kurzhaariger Vorstehhund; Deutsch Kurzhaar; Kurzhaar
Common Name: GSP;DK

Breed Registries
AKC
CKC
UKC
FCI
Yes
 Yes
 Yes
 Yes
Associated Disease Information
Disease Name Gene Name Disease Level (CIDD) Associated Links
Allergies      OMIM: 9123
Atopic dermatitis      OMIM: 9123
Behavioral abnormalities      OMIM: 9123
Calcinosis circumscripta      OMIM: 9123
Cellulitis (folliculitis and furunculosis)      OMIM: 9123
Cleft palate DLX6  OMIA:      OMIM: 9123
Coloboma      OMIM: 9123
Cystinuria SLC3A1  SLC7A9  OMIA:      OMIM: 9123
Atopic dermatitis      OMIM: 9123
Discoid lupus erythematosus      OMIM: 9123
Enostosis      OMIM: 9123
Eosinophilic panosteitis      OMIM: 9123
Epilepsy LGI2  DIRAS1  OMIA:      OMIM: 9123
Esophageal achalasia      OMIM: 9123
Gastric torsion      OMIM: 9123
Glycogen storage disease G6PC  GAA  PFKM  AGL  OMIA:      OMIM: 9123
Keratoacanthoma      OMIM: 9123
Lymphocytic thyroiditis      OMIM: 9123
Malabsorption syndrome      OMIM: 9123
Nasal pyoderma      OMIM: 9123
Osteochondritis dissecans      OMIM: 9123
Osteosarcoma      OMIM: 9123
Otitis externa      OMIM: 9123
Pancreatic insufficiency      OMIM: 9123
Renal cortical hypoplasia      OMIM: 9123
Fragmented coronoid process      OMIM: 9123
Hemangiosarcoma      OMIM: 9123
Osteochondrosis      OMIM: 9123
Osteochondrosis      OMIM: 9123
Cutaneous vasculopathy      OMIM: 9123
Ehlers Danlos syndrome      OMIM: 9123
Acral mutilation GDNF  have an increased incidence OMIA:      OMIM: 9123
Cataract HSF4  have an increased incidence OMIA:      OMIM: 9123
Cleft lip ADAMTS20  OMIA:      OMIM: 9123
Corneal dystrophy LOC489707  OMIA:      OMIM: 9123
Cutaneous asthenia      OMIM: 9123
Dermoid cyst      OMIM: 9123
Disorders of sexual development - sexual reversal HSD17B3  have an increased incidence OMIA:      OMIM: 9123
Elbow dysplasia      OMIM: 9123
Entropion have an increased incidence      OMIM: 9123
Hemivertebra have an increased incidence      OMIM: 9123
Hemophilia A F8  OMIA:      OMIM: 9123
Hemophilia B F9  OMIA:      OMIM: 9123
Hip dysplasia Most Important      OMIM: 9123
Hypothyroidism TPO  OMIA:      OMIM: 9123
Lens luxation ADAMTS17  OMIA:      OMIM: 9123
lupoid dermatosis have an increased incidence      OMIM: 9123
Lymphedema      OMIM: 9123
Lysosomal storage diseases      OMIM: 9123
Optic nerve hypoplasia      OMIM: 9123
Pannus      OMIM: 9123
Patent ductus arteriosus      OMIM: 9123
Pemphigus erythematosus      OMIM: 9123
Perianal fistulas      OMIM: 9123
Persistent right aortic arch      OMIM: 9123
Pituitary dwarfism POU1F1  LHX3  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
Immunoglobulin A deficiency      OMIM: 9123
Subaortic stenosis have an increased incidence      OMIM: 9123
Eversion of nictitating membrane have an increased incidence      OMIM: 9123
von Willebrand's disease VWF  have an increased incidence OMIA:      OMIM: 9123
X-linked muscular dystrophy may be inherited      OMIM: 9123
Associated SNP Information
There are no associated SNPs
Breed Standards
Reference
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