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220900
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DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM
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Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Eye Diseases
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Albinism
Albinism, Oculocutaneous
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Infant, Newborn, Diseases
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Oculocutaneous
Skin Diseases, Genetic
Albinism
Albinism, Oculocutaneous
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Oculocutaneous
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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