Pedigree database Hokkaido (Ainu-ken) » ARAMINE PINNESHIRI SUGIYAMA KENSHA

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Nick:ARAMINE PINNESHIRI SUGIYAMA KENSHA
Date of birth:00/00/0000
SexMale
Coat:
Colour:
Place of birth:JAPAN  JAPAN
Kennel (Breeder):
Breeder:
Living place :JAPAN  JAPAN
City:
Kennel (Owner):
Owner:
Father:SHOUTA KITAHIRO KOREISHI KENSHA
Mother:ICHIYUUME OTARU KAPPAI
Weight: kg.
Height: sm.
Eye color:
Bonitation code:
Character test:
Training:
Score:
Tatoo:
Organization:
Pedigree number:DOKENHO 125584
Chip:
Titles:

Inbreeding » Hide Photo Pedigree analysis

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

SHOUTA KITAHIRO KOREISHI KENSHA
SHOUTA KITAHIRO KOREISHI KENSHA
   JAPAN 
KATSUFUSA CHITOSE KANAMORI
KATSUFUSA CHITOSE KANAMORI
   JAPAN 
RIKIFUJI SAPPORO KOBAYASHI
RIKIFUJI SAPPORO KOBAYASHI
   JAPAN 
 Add
 Add
YUMA TOMIKAWATOYODA
YUMA TOMIKAWATOYODA
   JAPAN 
 Add
 Add
MARI CHITOSE KANAMORI
MARI CHITOSE KANAMORI
   JAPAN 
RIKUROU SHIRAOI MATSUYA
RIKUROU SHIRAOI MATSUYA
   JAPAN 
 Add
 Add
YUMI CHITOSE KANAMORI
YUMI CHITOSE KANAMORI
   JAPAN 
 Add
 Add
ICHIYUUME OTARU KAPPAI
ICHIYUUME OTARU KAPPAI
   JAPAN 
TAKEYUU OTARU KAPPAI
TAKEYUU OTARU KAPPAI
   JAPAN 
 Add---
---
 Add---
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CHIYOHIME GIFU SATSUMASOU
CHIYOHIME GIFU SATSUMASOU
   JAPAN 
 Add---
---
 Add---
---

Offsprings:

 HOKUYU HAKODATE SUZURANSOU    
 KOUJIN PINNESHIRI SUGIYAMA KENSHA    

Siblings:

Breedings:

 KOUGA PINNESHIRI SUGIYAMA KENSHA    
 MIHARU HAKODATE SUZURANSOU    
Patellar luxationPL<b>Patellar luxation</b>
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 Сiliагу DyskinesiaPCD<b>Primary Сiliагу Dyskinesia</b>
Brainstem Auditory Evoked ResponseBAER<b>BAER (Brainstem Auditory Evoked Response)</b>
Multi-Drug Resistance 1MDR1<b>Multi-Drug Resistance 1</b>
ThyroidTHYROID<b>Thyroid</b>
Copper ToxicosisCT<b>Copper Toxicosis</b>
Degenerative MyelopathyDM<b>Degenerative Myelopathy</b>
MucopolysaccharidosisMPS<b>Mucopolysaccharidosis</b>
Primary Lens LuxationPLL<b>Primary Lens Luxation</b>
Coat LengthCL<b>Coat Length</b>
Entlebucher Urinary SyndromeEUS<b>Entlebucher Urinary Syndrome</b>
CystinuriaCystinuria<b>Cystinuria</b>
Musladin-Leuke SyndromeMLS<b>Musladin-Leuke Syndrome</b>
Factor VIIFactor VII<b>Factor VII</b>
Neonatal Cerebellar Cortical DegenerationNCCD<b>Neonatal Cerebellar Cortical Degeneration</b>
Imerslund-Grasbeck syndromeIGS<b>Imerslund-Grasbeck syndrome</b>
von Willebrand diseasevWD<b>von Willebrand disease</b>
DwarfismDW<b>Dwarfism</b>
Exercise-induced collapseEIC<b>Exercise-induced collapse</b>
Hereditary nasal parakeratosisHNPK<b>Hereditary nasal parakeratosis</b>
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: 

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