Niveau 5 de descendance 

CH. Illuminati index d'ovilava

Bouledogue français

Bouledogue français - CH. Illuminati index d'ovilava

Publication : De L'Idylle Sacrée

Auteur : DANIELA

Description

ILLUMINATI INDEX D'OVILAVA est champion de Slovénie.

Il a était testé sur 211 maladie génétique.

Déjà papa, semence de qualité à plus de 80%.

Pedigree unique en France et ultra sélectif.

Male puissant de 28 cm et 13 kilo.
Bringé bien marqué avec ongle noir foncé. Et présente une belle queue et une tête puissante.

Les infos

Sexe mâle
Département 90 - Territoire de Belfort
Date de naissance 23/03/2019
Couleur BRINGE
Puce 25026***************
Inscrit au Livre d'origine Autriche
ADN OUI
Tares
2,8-dihydroxyadenine (DHA) Urolithiasis - Clear
Acral Mutilation Syndrome - Clear
Acute Respiratory Distress Syndrome - Clear
Adn - Fait
Alexander Disease - Clear
Amelogenesis Imperfecta - Clear
Bandera - Clear
Benign Familial Juvenile Epilepsy - Clear
Canine Leukocyte Adhesion Deficiency (CLAD), type III - Clear
Canine Multifocal Retinopathy 1 - Clear
Canine Multifocal Retinopathy 2 - Clear
Canine Multifocal Retinopathy 3 - Clear
Canine Scott Syndrome - Clear
Cerebellar Ataxia - Clear
Cerebellar Cortical Degeneration - Clear
Cerebellar Hypoplasia - Clear
Cerebral Dysfunction - Clear
Chondrodysplasia - Clear
Cleft Lip & Palate with Syndactyly - Clear
Cleft Palate - Clear
Collie Eye Anomaly (CEA) - Clear
Complement 3 Deficiency - Clear
Cone-Rod Dystrophy - Clear
Cone-Rod Dystrophy 1 - Clear
Cone-Rod Dystrophy 2 - Clear
Congenital Stationary Night Blindness (CSNB) - Clear
Craniomandibular Osteopathy - Clear
Cystic Renal Dysplasia and Hepatic Fibrosis - Clear
Cystinuria Type I-A - Clear
Cystinuria Type II-A - Clear
Dégénérescence myélopathie - Porteur sain
Demyelinating Neuropathy - Clear
Dental Hypomineralization - Clear
Dominant Progressive Retinal Atrophy - Clear
Epidermolytic Hyperkeratosis - Clear
Exercise-Induced Collapse - Clear
Factor VII Deficiency - Clear
Factor XI Deficiency - Clear
Fanconi Syndrome - Clear
Fetal Onset Neuroaxonal Dystrophy - Clear
Focal Non-Epidermolytic Palmoplantar Keratoderma - Clear
Glanzmann Thrombasthenia Type I - Clear
Glycogen Storage Disease Type Ia - Clear
Glycogen Storage Disease Type IIIa, (GSD IIIa) - Clear
Hemophilia B - Clear
Hereditary Elliptocytosis - Clear
Hereditary Footpad Hyperkeratosis - Clear
Hereditary Vitamin D-Resistant Rickets Type II - Clear
Hyperekplexia or Startle Disease - Clear
Hyperuricosuria - Clear
Hypocatalasia - Clear
Hypomyelination - Clear
Hypophosphatasia - Clear
Juvenile Laryngeal Paralysis and Polyneuropathy - Clear
Juvenile Myoclonic Epilepsy - Clear
L-2-Hydroxyglutaric Aciduria - Clear
Lagotto Storage Disease - Clear
Lamellar Ichthyosis - Clear
Ligneous Membranitis - Clear
Macrothrombocytopenia - Clear
May-Hegglin Anomaly - Clear
MDR1 Medication Sensitivity - Clear
Muscular Hypertrophy (Double Muscling) - Clear
Musladin-Lueke Syndrome - Clear
Myeloperoxidase Deficiency - Clear
Myotonia Congenita - Clear
Myotubular Myopathy - Clear
Nemaline Myopathy - Clear
Neonatal Cerebellar Cortical Degeneration - Clear
Neonatal Encephalopathy with Seizures - Clear
Neuroaxonal Dystrophy - Clear
Neuronal Ceroid Lipofuscinosis 1 - Clear
Neuronal Ceroid Lipofuscinosis 7 - Clear
Osteochondrodysplasia - Clear
P2RY12-associated Bleeding Disorder - Clear
Paroxysmal Dyskinesia - Clear
Persistent Müllerian Duct Syndrome - Clear
Phosphofructokinase Deficiency - Clear
Polycystic Kidney Disease - Clear
Prekallikrein Deficiency - Clear
Primary Ciliary Dyskinesia - Clear
Primary Lens Luxation - Clear
Progressive Early-Onset Cerebellar Ataxia - Clear
Progressive Retinal Atrophy Type III - Clear
Progressive Rod Cone Degeneration (prcd-PRA) - Clear
Protein Losing Nephropathy - Clear
Pyruvate Dehydrogenase Phosphatase 1 Deficiency - Clear
QT Syndrome - Clear
RADIO DU DOS - INDEME
Renal Cystadenocarcinoma and Nodular Dermatofibrosis - Clear
Rod-Cone Dysplasia 1 - Clear
Rod-Cone Dysplasia 1a - Clear
Rod-Cone Dysplasia 3 - Clear
ROTULE - 0/0
Sensory Ataxic Neuropathy - Clear
Sensory Neuropathy - Clear
Severe Combined Immunodeficiency - Clear
Severe Combined Immunodeficiency - Clear
Skeletal Dysplasia 2 - Clear
Spinocerebellar Ataxia (Late-Onset Ataxia) - Clear
Spinocerebellar Ataxia with Myokymia and/or Seizures - Clear
Spondylocostal Dysostosis - Clear

Ses titres

CHAMPION DE SLOVENIE

Ses résultats

2 EME EXC RCAC

CH. Illuminati index d'ovilava - 2 EME EXC RCAC

4.4.2021 - Sarajevo Spring

Ville : Sarajevo Bosnie - Juge : RADOVAN MAZALICA

2 EME EXC RCAC

CH. Illuminati index d'ovilava - 2 EME EXC RCAC

4.4.2021 - Sarajevo Spring

Ville : Sarajevo Bosnie - Juge : NEDIM SUTA

2 EME EXC RCAC

CH. Illuminati index d'ovilava - 2 EME EXC RCAC

3.4.2021 - Sarajevo Spring

Ville : Sarajevo Bosnie - Juge : Andras korozs

2 EME EXC RCAC

CH. Illuminati index d'ovilava - 2 EME EXC RCAC

3.4.2021 - Sarajevo Spring

Ville : Sarajevo Bosnie - Juge : Antonio Mracevic

2 ème excellent

CH. Illuminati index d'ovilava - 2 ème excellent

27.2.2021 - SKOPJE MACÉDOINE

Ville : SKOPJE MACÉDOINE - Juge : TORSTEN LEMMER

2 ème exc RCAC

CH. Illuminati index d'ovilava - 2 ème exc RCAC

27.2.2021 - SKOPJE MACÉDOINE

Ville : SKOPJE MACÉDOINE - Juge : TIJANA KONARD