Pedigree database Labrador Retriever » MALLARDHURN PAT

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Nick:MALLARDHURN PAT
Date of birth:00/00/0000
SexFemale
Colour:
Place of birth:---  ---
Kennel (Breeder):
Breeder:
Living place :---  ---
City:
Kennel (Owner):
Owner:
Father:POPPLETON LIEUTENANT
Mother:GUNSMITH SUSETTE
Weight: kg.
Height: sm.
Character test:
Training:
Score:
Tatoo:
Organization:
Pedigree number:
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Titles:

Inbreeding » Hide Photo Pedigree analysis

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

POPPLETON LIEUTENANT
POPPLETON LIEUTENANT
   --- 1949-03-19
Yellow
POPPLETON BEECH FLIGHT
POPPLETON BEECH FLIGHT
   --- 
POPPLETON GOLDEN FLIGHT
POPPLETON GOLDEN FLIGHT
   --- 1944-04-05
Yellow
POPPLETON GOLDEN RUSSET
POPPLETON GOLDEN RUSSET
   --- 
MODNEY CROCUS
MODNEY CROCUS
   --- 
LIME BEECH
LIME BEECH
   --- 
DURLEY BEECH
DURLEY BEECH
   --- 
LIDDLY LIMEJUICE
LIDDLY LIMEJUICE
   --- 
POPPLETON GOLDEN SUNRAY
POPPLETON GOLDEN SUNRAY
   --- 
POPPLETON GOLDEN MAJOR
POPPLETON GOLDEN MAJOR
   --- 1935-06-20
Yellow
POPPLETON BLACK LANCER
POPPLETON BLACK LANCER
   --- 
GOLDGLEAM OF POPPLETON
GOLDGLEAM OF POPPLETON
   --- 
POPPLETON GOLDEN DAWN
POPPLETON GOLDEN DAWN
   --- 
Yellow
ILTON ROGER
ILTON ROGER
   --- 
POPPLETON BLACK LILAC
POPPLETON BLACK LILAC
   --- 
BLACK
GUNSMITH SUSETTE
GUNSMITH SUSETTE
   --- 
GUNSMITH SILVER FLIGHT
GUNSMITH SILVER FLIGHT
   --- 
 Add---
---
 Add---
---
GUNSMITH SUGAR
GUNSMITH SUGAR
   --- 
 Add---
---
 Add---
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Offsprings:

 MALLARDHUM TWEED    
 REANACRE MALLARDHURN THUNDER    

Siblings:

Breedings:

 SANDYLANDS TWEED OF BLAIRCOURT    
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>
Primary Lens LuxationPLL<b>Primary Lens Luxation</b>
von Willebrand diseasevWD<b>von Willebrand disease</b>
Exercise-induced collapseEIC<b>Exercise-induced collapse</b>
Hereditary nasal parakeratosisHNPK<b>Hereditary nasal parakeratosis</b>
Centronuclear MyopathyCNM<b>Centronuclear Myopathy (CNM)</b>, group of congenital myopathies where cell nuclei are abnormally located in the center of skeletal muscle cells instead of their normal location at the periphery. Symptoms of CNM include severe hypotonia, hypoxia-requiring breathing assistance, and scaphocephaly.

Notes: 

Added: Karkela




 



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