MeSH Treeview
Query OMIM entry list
120970
CORD2
CONE-ROD DYSTROPHY 2
→
High-scoring List
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Nerve Tissue
Nerve Sheath Neoplasms
Neurofibroma
Neurofibromatoses
Neurofibromatosis 1
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Neurofibromatosis 1
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Labyrinth Diseases
Vestibular Diseases
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Neurocutaneous Syndromes
Neurofibromatoses
Neurofibromatosis 1
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Neurofibromatoses
Neurofibromatosis 1
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Vision Disorders
Color Vision Defects
Neuromuscular Diseases
Peripheral Nervous System Diseases
Neurofibromatosis 1
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinitis Pigmentosa
Ocular Motility Disorders
Nystagmus, Pathologic
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Refractive Errors
Myopia
Retinal Diseases
Retinal Degeneration
Macular Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Vision Disorders
Color Vision Defects
Night Blindness
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinitis Pigmentosa
Heredodegenerative Disorders, Nervous System
Neurofibromatoses
Neurofibromatosis 1
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Neurofibromatosis 1
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Optic Atrophy, Hereditary, Leber
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Nondisjunction, Genetic
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Sensation Disorders
Hearing Disorders
Hearing Loss
Hearing Loss, Sensorineural
Vision Disorders
Color Vision Defects
Database Center for Life Science