Blood
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Canine Leukocyte Adhesion Deficiency (CLAD), type III
Glanzmann Thrombasthenia Type I
P2RY12-associated Bleeding Disorder
von Willebrand's Disease, type 1
von Willebrand's Disease, type 2
von Willebrand's Disease, type 3
Phosphofructokinase Deficiency
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Dental
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Drug response
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Eye
Canine Multifocal Retinopathy 1
Canine Multifocal Retinopathy 2
Canine Multifocal Retinopathy 3
Progressive Retinal Atrophy Type III
Dominant Progressive Retinal Atrophy
X-Linked Progressive Retinal Atrophy 2
X-Linked Severe Combined Immunodeficiency
Severe Combined Immunodeficiency
Severe Combined Immunodeficiency
Lung
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Acute Respiratory Distress Syndrome
Metabolic
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Glycogen Storage Disease Type IIIa, (GSD IIIa)
Pyruvate Dehydrogenase Phosphatase 1 Deficiency
Mucopolysaccharidosis Type VII
Glycogen Storage Disease Type Ia
Mucopolysaccharidosis Type IIIA
Muscular Hypertrophy (Double Muscling)
Neuromuscular
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Congenital Myasthenic Syndrome
Congenital Myasthenic Syndrome
Early-Onset Progressive Polyneuropathy
Nervous system
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Hyperekplexia or Startle Disease
Neuronal Ceroid Lipofuscinosis 8
Spinocerebellar Ataxia (Late-Onset Ataxia)
Spinocerebellar Ataxia with Myokymia and/or Seizures
Neuronal Ceroid Lipofuscinosis 8
Neuronal Ceroid Lipofuscinosis 7
Juvenile Laryngeal Paralysis and Polyneuropathy
Spongy Degeneration with Cerebellar Ataxia
Cerebellar Cortical Degeneration
Neonatal Cerebellar Cortical Degeneration
Benign Familial Juvenile Epilepsy
Neuronal Ceroid Lipofuscinosis 1
Neonatal Encephalopathy with Seizures
Fetal Onset Neuroaxonal Dystrophy
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Reproductive system
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Persistent Müllerian Duct Syndrome
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Skeletal
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Hereditary Vitamin D-Resistant Rickets Type II
Cleft Lip & Palate with Syndactyly
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Skin
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Dystrophic Epidermolysis Bullosa
Hereditary Footpad Hyperkeratosis
Dystrophic Epidermolysis Bullosa
Focal Non-Epidermolytic Palmoplantar Keratoderma
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Urinary
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X-Linked Hereditary Nephropathy