Lab Fairytale´s Kiss the Sky

KØN:Tæve

FARVE: Sort, bærer gult EeBB

FØDT: 26.06.2025

REG.NR: DK09424/2025

ID: 208250000220733

Tests:

• Achromatopsia 2: Normal/Clear
• Alexander Disease: Normal/Clear
• Centronuclear Myopathy (CNM): Normal/Clear
• Congenital Cornification Disorder (ILVEN): Normal/Clear
• Congenital Myasthenic Syndrome (CMS): Normal/Clear 
• Cystinuria (Type I – A): Normal/Clear
• Degenerative Myelopathy Exon 2 (DM Exon 2):
• Dyserythropoietic Anemia and Myopathy Syndrome (DAMS): Normal/Clear
• Ehlers-Danlos Syndrome Type 1: Normal/Clear
• Exercise Induced Collapse, EIC: Normal/Clear
• Haemophilia A: Normal/Clear 
• HNPK:
• Hyperuricemia: Normal/Clear
• Laryngeal Paralysis and polyneuropathy: Normal/Cleaar
• Macular Corneal Dystrophy (MCD): Normal/Clear
• Malignant Hyperthermia (MH) : Normal/Clear
• Muscular Dystrophy (MD) – Labrador Retriever 1 : Normal Clear
• Muscular Dystrophy (MD) – Labrador Retriever 2: Normal Clear
• Muscular Dystrophy-Dystroglycanopathy (MDD): Normal Clear
• Myotonia Congenita : Normal Clear
• Narcolepsy: Normal Clear
• Obesity: Normal Clear
• Oculoskeletal Dysplasia 1 (OSD1) / Retinal Dysplasia (RD): Normal/Clear
• Progressive Retinal Atrophy (GR-PRA2): Normal/Clear
• Progressive Retinal Atrophy (prcd-PRA) : Normal/Clear
• Pyruvate Kinase Deficiency : Normal/Clear
• Skeletal Dysplasia 2 (SD2):Normal Clear
• Stargardt disease 1: Normal Clear
• Copper - Wilson Disease, ATP7B-related : Carrier
• X-linked Myotubular Myopathy (XLMTM)Hair Length - 1 FGF5 Autosomal Recessive S/S Short coat