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216900
ACHM2
ACHROMATOPSIA 2
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Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Color Vision Defects
Photophobia
Eye Diseases
Eye Diseases, Hereditary
Ocular Motility Disorders
Nystagmus, Pathologic
Retinal Diseases
Retinal Degeneration
Vision Disorders
Color Vision Defects
Photophobia
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Thalassemia
Hemoglobinopathies
Thalassemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Thalassemia
Eye Diseases, Hereditary
Hemoglobinopathies
Thalassemia
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Nondisjunction, Genetic
Uniparental Disomy
Translocation, Genetic
Disease Attributes
Disease Progression
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Vision Disorders
Color Vision Defects
Photophobia
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