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310600
ND
NORRIE DISEASE
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Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Epilepsies, Myoclonic
Epilepsy, Generalized
Spasms, Infantile
Seizures
Neurologic Manifestations
Dyskinesias
Myoclonus
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Intellectual Disability
Psychomotor Disorders
Neuromuscular Manifestations
Muscular Atrophy
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Vision Disorders
Blindness
Color Vision Defects
Sleep Disorders
Dyssomnias
Sleep Disorders, Intrinsic
Disorders of Excessive Somnolence
Narcolepsy
Cataplexy
Eye Diseases
Eye Abnormalities
Retinal Dysplasia
Eye Diseases, Hereditary
Retinal Dysplasia
Retinitis Pigmentosa
Lens Diseases
Cataract
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Retinal Detachment
Retinal Dysplasia
Retinopathy of Prematurity
Vitreoretinopathy, Proliferative
Vision Disorders
Blindness
Color Vision Defects
Vitreoretinopathy, Proliferative
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Glucosephosphate Dehydrogenase Deficiency
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Eye Abnormalities
Retinal Dysplasia
Fetal Diseases
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Glucosephosphate Dehydrogenase Deficiency
Chromosome Disorders
Eye Diseases, Hereditary
Retinal Dysplasia
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Infant, Newborn, Diseases
Infant, Premature, Diseases
Retinopathy of Prematurity
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sex Chromosome Aberrations
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Disease Progression
Signs and Symptoms
Body Weight
Birth Weight
Neurologic Manifestations
Dyskinesias
Myoclonus
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Intellectual Disability
Psychomotor Disorders
Neuromuscular Manifestations
Muscular Atrophy
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Vision Disorders
Blindness
Color Vision Defects
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