MeSH Treeview
Query OMIM entry list
311050
OPA2
OPTIC ATROPHY 2
→
High-scoring List
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Dementia
Huntington Disease
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Huntington Disease
Neurologic Manifestations
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Optic Nerve Diseases
Optic Atrophy
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Huntington Disease
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Database Center for Life Science
