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264900	-	PTA DEFICIENCY

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Neoplasms by Histologic Type

Leukemia, Lymphoid

Leukemia, T-Cell

Leukemia-Lymphoma, Adult T-Cell

Leukemia, Myeloid

Musculoskeletal Diseases

Nervous System Diseases

Central Nervous System Diseases

Basal Ganglia Diseases

Huntington Disease

Huntington Disease

Movement Disorders

Huntington Disease

Neurodegenerative Diseases

Heredodegenerative Disorders, Nervous System

Huntington Disease

Neurologic Manifestations

Neurobehavioral Manifestations

Intellectual Disability

Prader-Willi Syndrome

Ocular Hypertension

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Congenital Abnormalities

Abnormalities, Multiple

Prader-Willi Syndrome

Chromosome Disorders

Prader-Willi Syndrome

Genetic Diseases, Inborn

Blood Coagulation Disorders, Inherited

Factor XI Deficiency

Chromosome Disorders

Prader-Willi Syndrome

Genetic Diseases, X-Linked

Heredodegenerative Disorders, Nervous System

Huntington Disease

Metabolism, Inborn Errors

Lysosomal Storage Diseases

Nutritional and Metabolic Diseases

Metabolic Diseases

Metabolism, Inborn Errors

Lysosomal Storage Diseases

Nutrition Disorders

Prader-Willi Syndrome

Immune System Diseases

Immunoproliferative Disorders

Lymphoproliferative Disorders

Leukemia, Lymphoid

Leukemia, T-Cell

Leukemia-Lymphoma, Adult T-Cell

Animal Diseases

Pathological Conditions, Signs and Symptoms

Pathologic Processes

Disease Attributes

Blood Loss, Surgical

Intraoperative Complications

Blood Loss, Surgical

Postoperative Complications

Signs and Symptoms

Neurologic Manifestations

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