HOPSCOTCH Rosa Nyetshedd
- WALA Scale BY LINEAGE: AUSTRALIAN LABRADOODLE (ALD)
- DNA BREED IDENTIFICATION PROFILE BY PARENTAGE:
- 18.75% Toy Poodle / 12.5% Miniature Poodle / 41.875% Standard Poodle / 15.625% Labrador Retriever / 6.25% Cocker Spaniel / 6.25% Brittany Spaniel
HOPSCOTCH Rosa Nyetshedd
- CLEAR of all 180 Known Screenable Canine GENETIC Diseases by Parentage (as of April 2020)
- Colour: Strawberry Caramel
- Coat: Fleece
- Size / Height to Withers (Weight): MEDIUM
- LONG HAIR GENE (Canine C95F): POSITIVE
- HEREDITARY DISEASE DNA TEST RESULTS: Breed Specific Results Below:
- Canine Hyperuricosuria (SLC2A9): CLEAR by Parentage
- Centronuclear Myopathy (Labrador Retriever Type) (HACD1): CLEAR by Parentage
- Congenital Myasthenic Syndrome (Labrador Retriever Type) (COLQ): CLEAR by Parentage
- Cystinuria Labrador Retriever Type - CYN (SLC3A1): CLEAR by Parentage
- Degenerative Myelopathy - DM (SOD1): CLEAR by Parentage
- Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type) (SPTB): CLEAR by Parentage
- Exercise Induced Collapse (Retriever Type) (EIC): CLEAR by Parentage
- Gangliosidosis GM2 (Poodle Type) (HEXB): CLEAR by Parentage
- Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type) (SUV39H2): CLEAR by Parentage
- Hyperuricosuria: CLEAR by Parentage
- Macular Corneal Dystrophy (Labrador Type) (LOC4): CLEAR by Parentage
- Malignant Hyperthermia (RYR1): CLEAR by Parentage
- Mucopolysaccharidosis VI (Poodle Type): CLEAR by Parentage
- Myotubular Myopathy X-linked (MTM1): CLEAR by Parentage
- Myotubular Myopathy X-Linked (Labrador Retriever Type) (MTM1): CLEAR by Parentage
- Narcolepsy (Labrador) (HCRTR2): CLEAR by Parentage
- Neonatal Encephalopathy (Poodle Type) (ATF2): CLEAR by Parentage
- Progressive Rod Cone Degeneration - PRA (PRCD): CLEAR by Parentage
- Pyruvate Kinase Deficiency (Labrador Type) (PKLR): CLEAR by Parentage
- Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism) (COL11A2): CLEAR by Parentage
- von Willebrand's Disease Type I - VWDI (VWF): CLEAR by Parentage
