MeSH Treeview
Query OMIM entry list
302500
SCAX1
SPINOCEREBELLAR ATAXIA, X-LINKED 1
→
High-scoring List
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Multiple System Atrophy
Olivopontocerebellar Atrophies
Brain Damage, Chronic
Cerebral Palsy
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Movement Disorders
Multiple System Atrophy
Olivopontocerebellar Atrophies
Spinal Cord Diseases
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Multiple System Atrophy
Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
Paralysis
Ophthalmoplegia
Eye Diseases
Ocular Motility Disorders
Ophthalmoplegia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Sex Chromosome Aberrations
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
Paralysis
Ophthalmoplegia
Database Center for Life Science
