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
|
