Neurologic disorders
Acral mutilation syndrome
Alexander disease
Bandera's neonatal ataxia (BNAt)
Benign familial juvenile epilepsy (BFJE)
Cerebellar ataxia, KCNIP4-related
Cerebellar ataxia, RAB24-related
Cerebellar ataxia, SEL1L-related
Cerebellar cortical degeneration
CNS atrophy and cerebellar ataxia
Congenital myasthenic syndrome, CHAT-related
Congenital myasthenic syndrome, CHRNE-related
Congenital myasthenic syndrome, COLQ-related
Dandy-Walker-like malformation (cerebellar hypoplasia)
Degenerative myelopathy
Episodic falling syndrome (EFS)
Fetal-onset neuroaxonal dystrophy, MFN2-related
Generalized myoclonic epilepsy with photosensitivity
Hypomyelination
Juvenile-onset neuroaxonal dystrophy, TECPR2-related
Krabbe disease
L-2-hydroxyglutaricacidemia
Laryngeal paralysis and polyneuropathy
Laryngeal paralysis, RAPGEF6-related
Leigh-like subacute necrotizing encephalopathy (SNE)
Leukodystrophy, CYTB-related
Mitochondrial neurodegenerative disease with epileptic encephalopathy
Multiple system degeneration
Myoclonus epilepsy of Lafora
Narcolepsy
Neonatal encephalopathy with seizures
Neuroaxonal dystrophy, PLA2G6-related
Neuroaxonal dystrophy, VPS11-related
Neurodegenerative vacuolar storage disease
Neurological defects, MYO5A-related
Paroxysmal dyskinesia, PIGN-related
Paroxysmal dyskinesia, SOD1-related
Pelizaeus-Merzbacker disease (shaking pup disease)
Polyneuropathy, ARHGEF10-related
Polyneuropathy, GJA9-related
Polyneuropathy, NDRG1-related
Polyneuropathy, RAB3GAP1-related
Polyneuropathy, SBF2-related
Reduced ability to metabolize cognitive enhancer 5-(3-methoxyphenyl)-3-(5-methyl1,2,4-oxadiazol-3-yl)-2-oxo-1,2-dihydro-1,6-naphthyridine (AC-3933)
Sensory ataxic neuropathy
Sensory neuropathy
Spinal dysraphism
Spinocerebellar ataxia, CAPN1-related
Spinocerebellar ataxia, ITPR1-related
Spinocerebellar ataxia, KCNJ10-related
Spinocerebellar ataxia, SCN8A-related
Spinocerebellar ataxia, SLC12A6-related
Spinocerebellar ataxia, SPTBN2-related
Spongy degeneration with cerebellar ataxia (SDCA)
Spongy degeneration with cerebellar ataxia 1 (SDCA1)
Recommended by top vets with decades of experience
21 breeds
64 genetic health markers
50 genetic trait markers
