Pedigree database Golden Retriever » CESAR CHERRY V. D. KOATEN

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Nick:CESAR CHERRY V. D. KOATEN
Date of birth:00/00/0000
SexMale
Place of birth:---  ---
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Breeder:
Living place :---  ---
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Kennel (Owner):
Owner:
Father:KYON'S IKE MONTY
Mother:CHERRY DONNA V D KOATEN
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Inbreeding » Hide Photo Pedigree analysis

Generations: 3  4  5  6  7  8  9  10    Pedigree code 

KYON'S IKE MONTY
KYON'S IKE MONTY
   CANADA 
CHRYS-HAEFEN NEWQUAY ST IVES
CHRYS-HAEFEN NEWQUAY ST IVES
   CANADA 1979-02-04
SKYLON FONTAINE
SKYLON FONTAINE
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JOHN BLUND'S FASCINATION
JOHN BLUND'S FASCINATION
   --- 
NORAVON LUCIUS
NORAVON LUCIUS
   --- 1978-04-20
CAMROSE FABIUS TARQUIN
CAMROSE FABIUS TARQUIN
   --- 1975-03-07
NORAVON MELISSA
NORAVON MELISSA
   --- 1976-02-27
JOHN BLUND'S FRANCESKA
JOHN BLUND'S FRANCESKA
   --- 
PENGELLI LYSANDER
PENGELLI LYSANDER
   SWEDEN 1974-03-09
JOHN-BLUNDS AH-JA
JOHN-BLUNDS AH-JA
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CHERRY DONNA V D KOATEN
CHERRY DONNA V D KOATEN
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PRINCIPAL VAN MOSIESFUN
PRINCIPAL VAN MOSIESFUN
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JANOUSKA VAN SPOKENDAM
JANOUSKA VAN SPOKENDAM
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DONNA
DONNA
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MUSTA VAN 'T BLAUWE MEER
MUSTA VAN 'T BLAUWE MEER
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 Add
ANOUSCHKA VAN DE GOLDEN MIRACLES
ANOUSCHKA VAN DE GOLDEN MIRACLES
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Offsprings:

 TESSA NOESKA V.D. KOATEN    

Siblings:

Breedings:

 NOESKA    
Hip dysplasiaHD<b>Hip dysplasia</b>
Elbow dysplasiaED<b>Elbow dysplasia</b>
Progressive Rod-Cone Degeneration (PRA)PRA-prcd<b>Progressive Rod-Cone Degeneration (PRA)</b>
BiteПрикус<b>Bite</b>
Entlebucher Urinary SyndromeEUS<b>Entlebucher Urinary Syndrome</b>
Golden Retriever Progressive Retinal Atrophy GR-PRA1GR-PRA1<b>Golden Retriever Progressive Retinal Atrophy (GR-PRA1)</b> - Progressive retinal atrophy is characterized by bilateral degeneration of the retina resulting in progressive vision loss leading to total blindness. Clinical signs of PRA1 appear around 6 years of age.
Golden Retriever Progressive Retinal Atrophy GR-PRA2GR-PRA2<b>Golden Retriever Progressive Retinal Atrophy (GR-PRA2)</b> - Progressive retinal atrophy is characterized by bilateral degeneration of the retina resulting in progressive vision loss leading to total blindness. Clinical symptoms of PRA2 appear around 4 years of age.
IchthyosisICT<b>Ichthyosis</b>, is a family of genetic skin disorders characterized by dry, thickened, scaly skin.

Notes: 

Added: Karkela




 



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