Pedigree database Golden Retriever » SCARHOLME BRUNHILDA OF BLAELOCHSIDE

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Nick:SCARHOLME BRUNHILDA OF BLAELOCHSIDE
Date of birth:06/06/1987
SexFemale
Place of birth:---  ---
Kennel (Breeder):
Breeder:Sparrow
Living place :---  ---
City:
Kennel (Owner):
Owner:Hogg
Father:NINELL RAMBRUEN
Mother:NINELL MAGDALENA OF SCARHOLME
Bonitation code:
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Tatoo:
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Inbreeding » Hide Photo Pedigree analysis

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

NINELL RAMBRUEN
NINELL RAMBRUEN
   --- 1984-07-06
BETHROB BRACKEN
BETHROB BRACKEN
   --- 1980-09-08
KIMSGOLD DEAN
KIMSGOLD DEAN
   --- 
GARBANK GOLDEN ORIOLE
GARBANK GOLDEN ORIOLE
   --- 
NINELL MORWENNA
NINELL MORWENNA
   --- 1982-12-19
GYRIMA OLIVER
GYRIMA OLIVER
   --- 1985-10-16
NINELL FRANCHESCA
NINELL FRANCHESCA
   UNITED KINGDOM 1977-06-20
NINELL MAGDALENA OF SCARHOLME
NINELL MAGDALENA OF SCARHOLME
   --- 1982-12-28
GYRIMA OLIVER
GYRIMA OLIVER
   --- 1985-10-16
SANSUE TOBIAS
SANSUE TOBIAS
   --- 1971-03-27
GYRIMA GENEVIEVE
GYRIMA GENEVIEVE
   --- 
NINELL FRANCHESCA
NINELL FRANCHESCA
   UNITED KINGDOM 1977-06-20
NORTONWOOD FAUNUS
NORTONWOOD FAUNUS
   UNITED KINGDOM 1974-02-15
NINELL ADELINA
NINELL ADELINA
   --- 1972-11-15

Offsprings:

 BLAELOCHSIDE DREAM MAKER TO SCARHOLME    

Siblings:

Breedings:

 BETHROB BRACKEN    
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.
Cause of deathCoD<b>Cause of death</b>
Portosystemic shuntPSS<b>Portosystemic shunt (PSS)</b> - Anomaly of vessel development due to which the blood flow between different organs and the system bypasses liver.
Dilated cardiomyopathyDCM<b>Dilated cardiomyopathy (DCM)</b> - A condition in which the heart becomes enlarged and cannot pump blood effectively.

Notes: 

Added: Karkela




 



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