Morgan's Alpine Tikka TKE VHMA VSWB FITS FTI BCAT WC SPOT
Callname: Tikka
Gender: Female
Color: BLK
Coat Genotype: Black - Hidden Choc - EEBb
Whelp Date: 8/16/2021
Owner: Morgan Neutz
Breeder: Kristen Fritz
Gender: Female
Color: BLK
Coat Genotype: Black - Hidden Choc - EEBb
Whelp Date: 8/16/2021
Owner: Morgan Neutz
Breeder: Kristen Fritz
AKC Reg: SS29121205
UKC Reg: R349852
OFA Hips: OFA44F (LR-280603F44F-P-VPI)
Eye CERF/CAER: CLEAR/NORMAL (CAER)
OFA Elbow: OFEL44 (LR-EL127258F44-P-VPI)
CNM: Normal (Clear) - Pawprint/Orivet
EIC: Clear/Normal (LR-EIC9054/42F-PI)
PRA: Normal (Clear) - Pawprint/Orivet
OSD: Normal (Clear) - Pawprint/Orivet
Cardiac: Normal/Clear (Basic Cardiac)
D LOCUS: Clear/Non-Dilute (LR-DL4569/51F-PI)
Other Health Certifications:
CHIC #
CLEAR - Centronuclear Myopathy, Chondrodystrophy (CDDY and IVDD Risk), Cone Degeneration, Congenital Myasthenic Syndrome, Copper Toxicosis Type A & B, Cystinuria, Degenerative Myelopathy, Ehlers-Danlos Syndrome (Labrador Retriever Type Variant 1 & 2), Elliptocytosis, Exercise-Induced Collapse, Hereditary Nasal Parakeratosis, Hyperuricosuria, Ichthyosis, Laryngeal Paralysis and Polyneuropathy, Macular Corneal Dystrophy, Myotonia Congenita, Myotubular Myopathy 1, Narcolepsy, Progressive Retinal Atrophy, Cone-Rod Dystrophy 4, Progressive Rod-Cone Degeneration, Pyruvate Kinase Deficiency, Retinal Dysplasia/Oculoskeletal Dysplasia 1, Skeletal Dysplasia 2, Stargardt Disease, Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 1 & 2)
UKC Reg: R349852
OFA Hips: OFA44F (LR-280603F44F-P-VPI)
Eye CERF/CAER: CLEAR/NORMAL (CAER)
OFA Elbow: OFEL44 (LR-EL127258F44-P-VPI)
CNM: Normal (Clear) - Pawprint/Orivet
EIC: Clear/Normal (LR-EIC9054/42F-PI)
PRA: Normal (Clear) - Pawprint/Orivet
OSD: Normal (Clear) - Pawprint/Orivet
Cardiac: Normal/Clear (Basic Cardiac)
D LOCUS: Clear/Non-Dilute (LR-DL4569/51F-PI)
Other Health Certifications:
CHIC #
CLEAR - Centronuclear Myopathy, Chondrodystrophy (CDDY and IVDD Risk), Cone Degeneration, Congenital Myasthenic Syndrome, Copper Toxicosis Type A & B, Cystinuria, Degenerative Myelopathy, Ehlers-Danlos Syndrome (Labrador Retriever Type Variant 1 & 2), Elliptocytosis, Exercise-Induced Collapse, Hereditary Nasal Parakeratosis, Hyperuricosuria, Ichthyosis, Laryngeal Paralysis and Polyneuropathy, Macular Corneal Dystrophy, Myotonia Congenita, Myotubular Myopathy 1, Narcolepsy, Progressive Retinal Atrophy, Cone-Rod Dystrophy 4, Progressive Rod-Cone Degeneration, Pyruvate Kinase Deficiency, Retinal Dysplasia/Oculoskeletal Dysplasia 1, Skeletal Dysplasia 2, Stargardt Disease, Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 1 & 2)
**Check health clearances of this dog:
OFA Website - searchs by name (opens in new window & based on correct spelling of dog's name)***
The Kennel Club / BVA - British Clearances
OFA Website - searchs by name (opens in new window & based on correct spelling of dog's name)***
The Kennel Club / BVA - British Clearances
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