Pedigree database Golden Retriever » SUGARTYME SUNDANC CHRYS-HAEFEN

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Nick:SUGARTYME SUNDANC CHRYS-HAEFEN
Date of birth:00/00/0000
SexFemale
Place of birth:---  ---
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Breeder:
Living place :---  ---
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Father:CHRYS-HAEFEN THE NORSEMAN
Mother:KATIMAVIKS KISS ME KATE
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Inbreeding » Hide Photo Pedigree analysis

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

CHRYS-HAEFEN THE NORSEMAN
CHRYS-HAEFEN THE NORSEMAN
   CANADA 1982-00-00
MJAERUMHOGDA'S KYON FLYING SURPRISE
MJAERUMHOGDA'S KYON FLYING SURPRISE
   --- 
NORAVON LUCIUS
NORAVON LUCIUS
   --- 1978-04-20
MJAERUMHOGDA'S TOUCH OF CLASS
MJAERUMHOGDA'S TOUCH OF CLASS
   --- 
 Add---
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KATIMAVIKS KISS ME KATE
KATIMAVIKS KISS ME KATE
   --- 
KYON'S SYDNEY AT CHRYS-HAEFEN
KYON'S SYDNEY AT CHRYS-HAEFEN
   --- 
GOLDTREVE CAMPAIGNER
GOLDTREVE CAMPAIGNER
   --- 1985-02-19
 Add
KYON'S JESSICA AT KATIMAVIK
KYON'S JESSICA AT KATIMAVIK
   --- 
MJAERUMHOGDA'S KYON FLYING SURPRISE
MJAERUMHOGDA'S KYON FLYING SURPRISE
   --- 
CHRYS-HAEFEN LUCKY LADY
CHRYS-HAEFEN LUCKY LADY
   --- 

Offsprings:

 CHRYS-HAEFEN HEIDI'S LEGACY    

Siblings:

Breedings:

 MJAERUMHOGDA'S ZEDRICH    
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.

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