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172850
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PIEBALD TRAIT WITH NEUROLOGIC DEFECTS
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Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Cerebellar Ataxia
Movement Disorders
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Eye Diseases, Hereditary
Albinism
Piebaldism
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Fragile X Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Piebaldism
Skin Diseases, Genetic
Albinism
Piebaldism
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Albinism
Piebaldism
Skin Diseases, Genetic
Albinism
Piebaldism
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Piebaldism
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neurobehavioral Manifestations
Intellectual Disability
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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