Health & General information on ...

Scarlett - MistyWoods Gone With The Wind

Sire: CH Iron Hill's Trusted One 
Dam: MistyWoods Eclipse Of The Blood Moon
AKC # SS29977101
Born: September 14, 2021
OFA Hips:  EXCELLENT LR-274669E30F-P-VPI
OFA Elbow: NORMAL LR-EL121692F30-P-VPI
Eyes: NORMAL LR-EYE30907/31F-VPI
Advance Cardiac: NORMAL AUSC+ECHO LR-ACA4996/31F-VPI

DNA testing
Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant): Clear
Canine Elliptocytosis (SPTB Exon 30): Clear
Centronuclear Myopathy, CNM (PTPLA): Clear
Chondrodysplasia, CDPA (FGF4): Clear
Chondrodystrophy and Intervertebral Disc Disease, CDDY/IVDD, Type I IVDD (FGF4 retrogene - CFA12): Clear
Congenital Ichthyosis Type 1, ICH1 (PNPLA1): Clear Congenital Macrothrombocytopenia (Tubb1): Clear
Congenital Myasthenic Syndrome (CHAT): Clear
Copper Toxicosis (ATP7A, Labrador Retriever): Carrier
Copper Toxicosis (ATP7B, Labrador Retriever): Clear
Cystinuria Type I-A (SLC3A1): Clear
Degenerative Myelopathy, DM (SOD1A): Clear
Ehlers-Danlos Syndrome (Variants 1 and 2), EDS (TNXB): Clear
Elliptocytosis B-Spectrin (SPTB): Clear
Exercise-Induced Collapse (DNM1): Clear
Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8): Clear
Hereditary Footpad Hyperkeratosis (FAM83G): Clear
Hereditary Nasal Parakeratosis (SUV39H2): Clear
Hyperuricosuria (HU): Clear
Long Coat: Carrier
Laryngeal Paralysis, LP (RAPGEF6): Clear
Macular Corneal Dystrophy, MCD (CHST6): Clear
Malignant Hyperthermia (RYR1): Clear
Myotonia Congenita (CLCN1): Clear
Myotubular Myopathy 1, X-linked Myotubular Myopathy, XL-MTM (MTM1): Clear
Narcolepsy (Labrador Type, HCRTR2): Clear
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia, OSD1 (COL9A3, Labrador Retriever): Clear
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4: Clear
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration (PRCD): Clear
Progressive Rod-Cone Degeneration, PRCD (PRA-prcd): Clear
Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant): Clear
Skeletal Dysplasia 2, SD2 (COL11A2): Clear
Stargardt disease, STGD: Carrier
Ulrich-like Congenital Muscular Dystrophy (COL6A3, Labrador Variant): Clear