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Query OMIM entry list
605242
USH1C
USH1C GENE
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Neoplasms
Hamartoma
Musculoskeletal Diseases
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Polydactyly
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Labyrinth Diseases
Vestibular Diseases
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Hypothalamic Diseases
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Polydactyly
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Retinitis Pigmentosa
Nutritional and Metabolic Diseases
Metabolic Diseases
Glucose Metabolism Disorders
Hyperinsulinism
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Inversion
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
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