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Miniature Poodle Detail Information
General Information

iDog Breed Number: CB268
Original: France&Germany
Personality:
Energy Level: Though possessing an air of distinction and dignity, the Miniature Poodle is an active dog that fits well into city living. A daily walk satisfies his exercise requirements.
Grooming: Not a job for the faint of heart, Poodle grooming is an acquired art. The breed may be shown in ‘puppy’ clip if under a year, the ‘English saddle’ clip or the ‘continental’ clip. All three require scissoring and clipping along with copious brushing and combing. Just for the record, Poodles may also be shown corded like the Puli but few are kept in that coat.
Trainability: Poodles are extremely intelligent and are easily trained. They are agile and graceful as well as smart, and they enjoy and excel in a variety of canine sports, including agility, obedience, and tracking. They are excellent water retrievers and also compete in dock diving and retriever hunt tests. Poodles are very people oriented, and if your training routines are fun and positive, they are quick to please you. Just be sure that you are being consistent with what you ask.
Height: 25-38 cm
Weight: 4.5-6.8kg
Life Expectancy: 10-18 years
History:


Web Source Name: Miniature Poodle from CKC

Breed Registries
AKC
CKC
UKC
FCI
Yes
 Yes
 No No
Associated Disease Information
Disease Name Gene Name Disease Level (CIDD) Associated Links
Achondroplasia      OMIM: 9123
Allergies      OMIM: 9123
Basal cell tumor      OMIM: 9123
Behavioral abnormalities      OMIM: 9123
Cerebrospinal demyelination      OMIM: 9123
Atopic dermatitis      OMIM: 9123
Distichiasis      OMIM: 9123
Ectopic ureters      OMIM: 9123
Epilepsy LGI2  DIRAS1  OMIA:      OMIM: 9123
Epiphora      OMIM: 9123
Epiphyseal dysplasia      OMIM: 9123
Granulomatous sebaceous adenitis      OMIM: 9123
Hemeralopia      OMIM: 9123
Hyposomatotropism      OMIM: 9123
Iris atrophy      OMIM: 9123
Osteochondritis dissecans      OMIM: 9123
Osteogenesis imperfecta SERPINH1  COL1A2  COL1A1  OMIA:      OMIM: 9123
Otitis externa      OMIM: 9123
Retinal detachment      OMIM: 9123
Sebaceous gland tumor      OMIM: 9123
Squamous cell carcinoma      OMIM: 9123
Osteochondrosis      OMIM: 9123
Atopy have an increased incidence      OMIM: 9123
Cataract HSF4  have an increased incidence OMIA:      OMIM: 9123
Cerebellar cortical abiotrophy have an increased incidence      OMIM: 9123
Coagulation (bleeding) disorders P2RY12  have an increased incidence OMIA:      OMIM: 9123
congenital hypotrichosis have an increased incidence      OMIM: 9123
Corneal dystrophy LOC489707  have an increased incidence OMIA:      OMIM: 9123
Cryptorchidism have an increased incidence      OMIM: 9123
Deafness have an increased incidence      OMIM: 9123
Diabetes mellitus have an increased incidence      OMIM: 9123
Ectodermal defects have an increased incidence      OMIM: 9123
Entropion have an increased incidence      OMIM: 9123
Glaucoma ADAMTS10  NEB  ADAMTS17  have an increased incidence OMIA:      OMIM: 9123
Globoid cell leukodystrophy GALC  have an increased incidence OMIA:      OMIM: 9123
Growth hormone-responsive dermatosis; adrenal sex hormone responsive dermatosis have an increased incidence      OMIM: 9123
Hemophilia A F8  OMIA:      OMIM: 9123
Hyperadrenocorticism or Cushing's disease have an increased incidence      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
Lacrimal duct atresia      OMIM: 9123
Intervertebral disc disease FGF4 retrogene in CFA12  have an increased incidence OMIA:      OMIM: 9123
Keratoconjunctivitis sicca FAM83H  have an increased incidence OMIA:      OMIM: 9123
Legg-Perthes disease have an increased incidence      OMIM: 9123
Lupus erythematosus (systemic, cutaneous/discoid) have an increased incidence      OMIM: 9123
Lysosomal storage diseases      OMIM: 9123
Microphthalmia have an increased incidence      OMIM: 9123
Mitral valve dysplasia Most Important      OMIM: 9123
Myasthenia gravis      OMIM: 9123
Optic nerve hypoplasia have an increased incidence      OMIM: 9123
Pannus      OMIM: 9123
Patella luxation Most Important      OMIM: 9123
Patent ductus arteriosus have an increased incidence      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
Pyruvate kinase deficiency PKLR  have an increased incidence OMIA:      OMIM: 9123
Retinal dysplasia have an increased incidence      OMIM: 9123
Sebaceous adenitis have an increased incidence      OMIM: 9123
Eversion of nictitating membrane have an increased incidence      OMIM: 9123
Urolithiasis (stones) SLC2A9  have an increased incidence OMIA:      OMIM: 9123
Ventricular septal defect      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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