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172800
PBT
PIEBALD TRAIT
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Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Colonic Diseases
Megacolon
Respiratory Tract Diseases
Nose Diseases
Nose Deformities, Acquired
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nose Diseases
Nose Deformities, Acquired
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Eye Diseases
Eye Diseases, Hereditary
Albinism
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Macrocytic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Waardenburg Syndrome
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Albinism
Piebaldism
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
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease
Syndrome
Growth Disorders
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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