Blood

Canine Leukocyte Adhesion Deficiency (CLAD), type III

Glanzmann Thrombasthenia Type I

P2RY12-associated Bleeding Disorder

Hereditary Elliptocytosis

Hemophilia A

Pyruvate Kinase Deficiency

Prekallikrein Deficiency

Macrothrombocytopenia

Factor XI Deficiency

Hemophilia A

Factor VII Deficiency

Canine Scott Syndrome

Trapped Neutrophil Syndrome

von Willebrand's Disease, type 1

von Willebrand's Disease, type 2

von Willebrand's Disease, type 3

Phosphofructokinase Deficiency

May-Hegglin Anomaly

Hemophilia B

Dental

Amelogenesis Imperfecta

Dental Hypominera

 

Drug response

Multidrug Resistance 1

Eye

Cone Degeneration

Canine Multifocal Retinopathy 1

Canine Multifocal Retinopathy 2

Canine Multifocal Retinopathy 3

Progressive Retinal Atrophy

Progressive Retinal Atrophy Type III

Cone-Rod Dystrophy 2

Dominant Progressive Retinal Atrophy

Progressive Retinal Atrophy

Primary Open Angle Glaucoma

Primary Open Angle Glaucoma

Cone-Rod Dystrophy 1

Rod-Cone Dysplasia 1

Rod-Cone Dysplasia 1a

Rod-Cone Dysplasia 3

X-Linked Progressive Retinal Atrophy 2

Primary Lens Luxation

Cone-Rod Dystrophy

QT Syndrome

Dilated Cardiomyopathy

Congenital Hypothyroidism

X-Linked Severe Combined Immunodeficiency

Complement 3 Deficiency

Severe Combined Immunodeficiency

Myeloperoxidase Deficiency

Severe Combined Immunodeficiency

 

Lung

Acute Respiratory Distress Syndrome

Primary Ciliary Dyskinesia

 

 

Metabolic

Glycogen Storage Disease Type IIIa, (GSD IIIa)

Hypocatalasia

Imerslund-Gräsbeck Syndrome

Imerslund-Gräsbeck Syndrome

Pyruvate Dehydrogenase Phosphatase 1 Deficiency

Mucopolysaccharidosis Type VII

Glycogen Storage Disease Type Ia

Mucopolysaccharidosis Type IIIA

X-Linked Myotubular Myopathy

Muscular Hypertrophy (Double Muscling)

Muscular Dystrophy 

Nemaline Myopathy

Muscular Dystrophy

Myotonia Congenita

Centronuclear Myopathy

 

 

Neuromuscular

GM2 Gangliosidosis

Congenital Myasthenic Syndrome

Exercise-Induced Collapse

Globoid Cell Leukodystrophy

Congenital Myasthenic Syndrome

Early-Onset Progressive Polyneuropathy

Episodic Falling Syndrome

 

 

Nervous system

L-2-Hydroxyglutaric Aciduria

Hyperekplexia or Startle Disease

Hypomyelination

Encephalopathy

Neuronal Ceroid Lipofuscinosis 8

X-Linked Tremors

Cerebellar Ataxia

Spinocerebellar Ataxia (Late-Onset Ataxia)

Spinocerebellar Ataxia with Myokymia and/or Seizures

Lagotto Storage Disease

Sensory Ataxic Neuropathy

L-2-Hydroxyglutaric Aciduria

Degenerative Myelopathy

Neuronal Ceroid Lipofuscinosis 8

Acral Mutilation Syndrome

Cerebellar Hypoplasia

Neuronal Ceroid Lipofuscinosis 7

Juvenile Laryngeal Paralysis and Polyneuropathy

Cerebral Dysfunction

Neuroaxonal Dystrophy

Paroxysmal Dyskinesia

Spongy Degeneration with Cerebellar Ataxia

Juvenile Myoclonic Epilepsy

Cerebellar Cortical Degeneration

Sensory Neuropathy

Alexander Disease

Narcolepsy

Neonatal Cerebellar Cortical Degeneration

Bandera's Neonatal Ataxia

Benign Familial Juvenile Epilepsy

Neuronal Ceroid Lipofuscinosis 1

Neonatal Encephalopathy with Seizures

Fetal Onset Neuroaxonal Dystrophy

 

 

Reproductive system

Persistent Müllerian Duct Syndrome

 

Skeletal

Musladin-Lueke Syndrome

Skeletal Dysplasia 2

Craniomandibular Osteopathy

Hereditary Vitamin D-Resistant Rickets Type II

Osteogenesis Imperfecta

Osteochondrodysplasia

Cleft Lip & Palate with Syndactyly

Cleft Palate

Spondylocostal Dysostosis

Osteogenesis Imperfecta

Chondrodysplasia

 

Skin

Lamellar Ichthyosis

Dystrophic Epidermolysis Bullosa

Epidermolytic Hyperkeratosis

Hereditary Footpad Hyperkeratosis

Dystrophic Epidermolysis Bullosa

Focal Non-Epidermolytic Palmoplantar Keratoderma

Ichthyosis

Ligneous Membranitis

Ichthyosis

X-Linked Ectodermal Dysplasia

 

Urinary

Polycystic Kidney Disease

X-Linked Hereditary Nephropathy

Renal Cystadenocarcinoma and Nodular Dermatofibrosis

Fanconi Syndrome

Protein Losing Nephropathy

Cystinuria Type II-A

Xanthinuria

Hyperuricosuria

Cystinuria Type I-A

X-Linked Hereditary Nephropathy