Base de datos de pedigrí Golden Retriever » JAYE OF PANDORAINN

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Nombre:JAYE OF PANDORAINN
Fecha de nacimiento:00/00/0000
SexoMacho
Lugar de nacimiento:UNITED KINGDOM  UNITED KINGDOM
Centro de acogida (Criador):
Criador:
Domicilio:---  ---
Ciudad:
Centro de acogida (Dueño):
Dueño:
Padre:GLEAM OF MORINDA
Madre:JUNO TOO OF PANDORAINN
Código de bonificación:
Test de carácter:
Adiestramiento:
Sello:
Organización:
№ del árbol genealógico:
Chip:
Títulos:

Endogamia » Ocultar la imagen El análisis del árbol genealógico

Generaciones: 3  4  5  6  7  8  9  10    Código del árbol genealógico 

GLEAM OF MORINDA
GLEAM OF MORINDA
   --- 
JOKER OF MORINDA
JOKER OF MORINDA
   --- 
DORCAS GLORIOUS OF SLAT
DORCAS GLORIOUS OF SLAT
   --- 1943-07-04
DORCAS BRUIN
DORCAS BRUIN
   --- 1937-03-25
STELLA OF SLAT
STELLA OF SLAT
   --- 
GOLDEN GIRL OF MORINDA
GOLDEN GIRL OF MORINDA
   --- 1943-09-19
DUKE OF ELSIVILLE
DUKE OF ELSIVILLE
   --- 
SANDRA OF INGLEDENE
SANDRA OF INGLEDENE
   --- 
 Añadir------
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JUNO TOO OF PANDORAINN
JUNO TOO OF PANDORAINN
   --- 
 Añadir------
---
------
---
 Añadir------
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Sucesores:

 JASPER OF FIVEWINDS    

Hermanastros:

 SYNSPUR JILL    

Cruzas:

     
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.

Notas: 

Añadió: leto




 



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