These pups are guaranteed to not be affected by the following:
Coagulation factor VII deficiencyElliptocytosis
Leukocyte adhesion deficiency, type III
May-Hegglin anomaly
P2RY12 receptor platelet disorder
Prekallikrein deficiency
Pyruvate kinase deficiency
Von Willebrand disease
Renal cystadenocarcinoma and nodular dermatofibrosis
Amelogenesis imperfecta
Multidrug resistance 1
Cone degeneration
Congenital stationary night blindness
Dry eye curly coat syndrome
Early retinal degeneration
Hereditary cataracts
Multifocal retinopathy 1
Multifocal retinopathy 2
Multifocal retinopathy 3
Primary lens luxation
Primary open angle glaucoma
Progressive retinal atrophy, Cone-rod dystrophy
Progressive retinal atrophy
Progressive rod-cone degeneration
Progressive retinal atrophy Rod-cone dysplasia 3
Progressive retinal atrophy, generalized
Complement 3 deficiency
Primary ciliary dyskinesia
Trapped neutrophil syndrome
Gallbladder mucoceles
Glycogen storage disease IIIa
Adult-onset neuronal ceroid lipofuscinosis
Glycogen storage disease IIIa
Glycogen storage disease Ia
Glycogen storage disease VII
Mucopolysaccharidosis I
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Pompe disease
Pyruvate dehydrogenase deficiency
Pyruvate kinase deficiency
Glycogen storage disease IIIa
Mucopolysaccharidosis I
Musladin-Lueke syndrome
Myotubular myopathy 1
Osteochondrodysplasia
Pompe disease
Skeletal dysplasia 2
Adult-onset neuronal ceroid lipofuscinosis
Benign familial juvenile epilepsy
Congenital myasthenic syndrome
Degenerative myelopathy
Episodic falling syndrome
Exercise-induced collapse
Juvenile Laryngeal Paralysis and Polyneuropathy
Late onset ataxia
Mucopolysaccharidosis I
Musladin-Lueke syndrome
Narcolepsy
Neonatal cerebellar cortical degeneration
Neonatal encephalopathy with seizures
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Sensory ataxic neuropathy
Spinocerebellar ataxia
Startle disease
Primary ciliary dyskinesia
Primary ciliary dyskinesia
Anhidrotic ectodermal dysplasia
Dry eye curly coat syndrome
Dystrophic epidermolysis bullosa
Ectodermal dysplasia
Epidermolytic hyperkeratosis
Hereditary nasal parakeratosis
Renal cystadenocarcinoma and nodular dermatofibrosis
Fanconi syndrome
Hyperuricosuria
Persistent Müllerian duct syndrome
Primary ciliary dyskinesia
Primary hyperoxaluria
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