Pedigree database Finnish Lapphund » CURKE X001275

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Nick:CURKE X001275
Date of birth:10/10/1969
SexMale
Coat:
Colour:
Place of birth:---  ---
Kennel (Breeder):
Breeder:
Living place :---  ---
City:
Kennel (Owner):
Owner:
Father:CEMMU U000012
Mother:MUSTI U000013
Weight: kg.
Height: sm.
Eye color:
Bonitation code:
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Inbreeding » Hide Photo Pedigree analysis

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

CEMMU U000012
CEMMU U000012
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MUSTI U000013
MUSTI U000013
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Offsprings:

 POROMIEHEN AHKU X004376    
 POROMIEHEN CALMU    
 POROMIEHEN CEMMU    
 POROMIEHEN JUUSO    
 POROMIEHEN MOTTERI    
 POROMIEHEN MUSTI    
 POROMIEHEN NAPPE    
 POROMIEHEN NASTI    
 POROMIEHEN PARKKU    
 POROMIEHEN RISKU    
 POROMIEHEN RISLA    
 POROMIEHEN RIUKU    
 POROMIEHEN RUSKA    
 POROMIEHEN TIKKAL    
 POROMIEHEN ZUKU X000877    

Siblings:

Breedings:

 POROMIEHEN CEEPU    
 POROMIEHEN HURRA    
 POROMIEHEN KIELA    
 POROMIEHEN NASTI    
 POROMIEHEN PARKKU    
 POROMIEHEN RAUNA    
 POROMIEHEN TESSU    
 POROMIEHEN TIKKAL    
 RIUKU SF18303A78    
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: 

Added: Anne Holopainen




 



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