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1 Multiple System Degeneration Muscular Dystrophy Musladin–Lueke Syndrome Mycobacterium Avium Susceptibility Myeloperoxidase deficiency Myostatin Deficiency Myotonia Congenita Myotonia Hereditaria Myotubular Myopathy Narcolepsy Necrotizing Meningoencephalitis Nemaline Myopathy Neonatal Ataxia Neonatal Cerebellar Cortical Degeneration Neonatal Encephalopathy Neonatal Encephalopathy with Seizures Neonatal Neuroaxonal Dystrophy Neuroaxonal Dystrophy Neurodegenerative Vacuolar Storage Disease Neuronal Ceroid Lipofuscinosis 1, 2, 4a, 5, 6, 7, 8, 10, A, MFSD8 Niemann‐Pick C Oculoskeletal Dysplasia Osteochondrodysplasia Osteochondromatosis Osteogenesis Imperfecta P2Y12 Receptor Platelet Disorder Palmoplantar Keratoderma Pancreatitis (marker) Pannus (marker) Paroxysmal Dyskinesia Periodic Fever Syndrome Persistent Mullerian Duct Syndrome Phosphofructokinase Deficiency Pituitary Dwarfism Platelet Dysfunction Platelet Procoagulant Deficiency – Scott Syndrome Polycystic Kidney Disease Polyneuropathy Pompe Disease Porphyria Postoperative Hemorrhage Prekallikrein Deficiency Primary Ciliary Dyskinesia Primary Lens Luxation Primary Open Angle Glaucoma Progress Retinal Atrophy ‐ crd4/cord1 Progressive Neuronal Abiotrophy Progressive Retinal Atrophy ‐ AD/RHO Progressive Retinal Atrophy ‐ CNGA Progressive Retinal Atrophy ‐ CNGB1 Progressive Retinal Atrophy ‐ crd (1, 2, 3, 4) Progressive Retinal Atrophy ‐ erd Progressive Retinal Atrophy ‐ Golden Retriever (1 & 2) Progressive Retinal Atrophy ‐ IG‐PRA1 Progressive Retinal Atrophy ‐ Late Onset Progressive Retinal Atrophy ‐ rcd (1, 1a, 2, 3, 4) Progressive Retinal Atrophy ‐ RdAc Progressive Retinal Atrophy ‐ Rdy Progressive Retinal Atrophy ‐ SAG Progressive Retinal Atrophy ‐ Type 1, 3, 4 Progressive Retinal Atrophy ‐ Type A, B Progressive Retinal Atrophy ‐ Type III Progressive Retinal Atrophy ‐ X‐linked Progressive Rod Cone Degeneration (prcd) Protein‐Losing Nephropathy Pyruvate Dehydrogenase Phosphatase Deficiency Pyruvate Kinase Deficiency Raine Syndrome Dental Hypomineralization Renal Cystadenocarcinoma and Nodular Dermatofibrosis Renal Dysplasia Retinal Degeneration Rickets Rod‐Cone Dysplasia 1, 1a, 3 Sanfilippo Syndrome Type A / Mucopolysaccharidosis IIIA (Dachshund Type) Scott Syndrome Sensory Ataxic Neuropathy Sensory Neuropathy Severe Combined Immunodeficiency (Autosomal) Severe Combined Immunodeficiency (X‐linked) Shaking Puppy Shar‐Pei Inflammatory Disease Short Tail (Brachyury) Skeletal Dysplasia Spinal Dysraphism Spinal Muscular Atrophy Spinocerebellar Ataxia Spondylocostal Dysostosis Spongiform Leukoencephalomyelopathy Spongy Degeneration with Cerebellar Ataxia (1 & 2) Stargardt Disease Startle Disease Subacute Necrotizing Encephalopathy Thrombopathia Trapped Neutrophil Syndrome van den Ende‐Gupta Syndrome von Willebrand Disease Types I, II, and III Xanthuria Type 1a, 2a, 2b X‐Linked Ectodermal Dysplasia X‐Linked Generalized Tremor Syndrome

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