MeSH Treeview
Query OMIM entry list
304020
CORDX1
CONE-ROD DYSTROPHY, X-LINKED, 1
→
High-scoring List
Nervous System Diseases
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Color Vision Defects
Photophobia
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Refractive Errors
Myopia
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Vision Disorders
Color Vision Defects
Night Blindness
Photophobia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Color Vision Defects
Photophobia
Database Center for Life Science