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245200	-	KRABBE DISEASE

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Bacterial Infections and Mycoses

Bacterial Infections

Gram-Negative Bacterial Infections

Bartonellaceae Infections

Bartonella Infections

Cat-Scratch Disease

Cat-Scratch Disease

Neoplasms by Histologic Type

Neoplasms, Connective and Soft Tissue

Neoplasms, Connective Tissue

Neoplasms, Fibrous Tissue

Neoplasms, Germ Cell and Embryonal

Neuroectodermal Tumors

Neoplasms, Neuroepithelial

Neoplasms, Glandular and Epithelial

Neoplasms, Neuroepithelial

Neoplasms, Nerve Tissue

Neuroectodermal Tumors

Neoplasms, Neuroepithelial

Musculoskeletal Diseases

Muscular Diseases

Muscle Spasticity

Nervous System Diseases

Autoimmune Diseases of the Nervous System

Demyelinating Autoimmune Diseases, CNS

Diffuse Cerebral Sclerosis of Schilder

Central Nervous System Diseases

Leukoencephalopathies

Demyelinating Autoimmune Diseases, CNS

Diffuse Cerebral Sclerosis of Schilder

Hereditary Central Nervous System Demyelinating Diseases

Adrenoleukodystrophy

Leukodystrophy, Globoid Cell

Leukodystrophy, Metachromatic

Movement Disorders

Demyelinating Diseases

Demyelinating Autoimmune Diseases, CNS

Diffuse Cerebral Sclerosis of Schilder

Hereditary Central Nervous System Demyelinating Diseases

Adrenoleukodystrophy

Leukodystrophy, Globoid Cell

Leukodystrophy, Metachromatic

Neurologic Manifestations

Neurobehavioral Manifestations

Intellectual Disability

Mental Retardation, X-Linked

Adrenoleukodystrophy

Neuromuscular Manifestations

Muscle Hypertonia

Muscle Spasticity

Sensation Disorders

Vision Disorders

Neuromuscular Diseases

Peripheral Nervous System Diseases

Vision Disorders

Female Urogenital Diseases and Pregnancy Complications

Pregnancy Complications

Hemic and Lymphatic Diseases

Lymphatic Diseases

Histiocytosis, Non-Langerhans-Cell

Niemann-Pick Diseases

Cat-Scratch Disease

Lymphoproliferative Disorders

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Congenital Abnormalities

Chromosome Disorders

Genetic Diseases, Inborn

Chromosome Disorders

Genetic Diseases, X-Linked

Mental Retardation, X-Linked

Adrenoleukodystrophy

Heredodegenerative Disorders, Nervous System

Mental Retardation, X-Linked

Adrenoleukodystrophy

Metabolism, Inborn Errors

Brain Diseases, Metabolic, Inborn

Hereditary Central Nervous System Demyelinating Diseases

Adrenoleukodystrophy

Leukodystrophy, Globoid Cell

Leukodystrophy, Metachromatic

Lysosomal Storage Diseases, Nervous System

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Gangliosidosis, GM1

Sandhoff Disease

Leukodystrophy, Globoid Cell

Niemann-Pick Diseases

Leukodystrophy, Metachromatic

Peroxisomal Disorders

Adrenoleukodystrophy

Carbohydrate Metabolism, Inborn Errors

Mucopolysaccharidoses

Mucopolysaccharidosis I

Lipid Metabolism, Inborn Errors

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Gangliosidosis, GM1

Leukodystrophy, Globoid Cell

Niemann-Pick Diseases

Leukodystrophy, Metachromatic

Lysosomal Storage Diseases

Lysosomal Storage Diseases, Nervous System

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Gangliosidosis, GM1

Leukodystrophy, Globoid Cell

Niemann-Pick Diseases

Leukodystrophy, Metachromatic

Mucopolysaccharidoses

Mucopolysaccharidosis I

Peroxisomal Disorders

Adrenoleukodystrophy

Skin and Connective Tissue Diseases

Connective Tissue Diseases

Mucopolysaccharidoses

Mucopolysaccharidosis I

Nutritional and Metabolic Diseases

Metabolic Diseases

Brain Diseases, Metabolic

Brain Diseases, Metabolic, Inborn

Hereditary Central Nervous System Demyelinating Diseases

Adrenoleukodystrophy

Leukodystrophy, Globoid Cell

Leukodystrophy, Metachromatic

Lysosomal Storage Diseases, Nervous System

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Gangliosidosis, GM1

Sandhoff Disease

Leukodystrophy, Globoid Cell

Niemann-Pick Diseases

Leukodystrophy, Metachromatic

Peroxisomal Disorders

Adrenoleukodystrophy

Calcium Metabolism Disorders

Lipid Metabolism Disorders

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Gangliosidosis, GM1

Leukodystrophy, Globoid Cell

Niemann-Pick Diseases

Leukodystrophy, Metachromatic

Metabolism, Inborn Errors

Brain Diseases, Metabolic, Inborn

Hereditary Central Nervous System Demyelinating Diseases

Adrenoleukodystrophy

Leukodystrophy, Globoid Cell

Leukodystrophy, Metachromatic

Lysosomal Storage Diseases, Nervous System

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Gangliosidosis, GM1

Sandhoff Disease

Leukodystrophy, Globoid Cell

Niemann-Pick Diseases

Leukodystrophy, Metachromatic

Peroxisomal Disorders

Adrenoleukodystrophy

Carbohydrate Metabolism, Inborn Errors

Mucopolysaccharidoses

Mucopolysaccharidosis I

Lipid Metabolism, Inborn Errors

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Gangliosidosis, GM1

Leukodystrophy, Globoid Cell

Niemann-Pick Diseases

Leukodystrophy, Metachromatic

Lysosomal Storage Diseases

Lysosomal Storage Diseases, Nervous System

Sphingolipidoses

Gangliosidoses, GM2

Sandhoff Disease

Gangliosidosis, GM1

Leukodystrophy, Globoid Cell

Niemann-Pick Diseases

Leukodystrophy, Metachromatic

Mucopolysaccharidoses

Mucopolysaccharidosis I

Peroxisomal Disorders

Adrenoleukodystrophy

Endocrine System Diseases

Adrenal Gland Diseases

Adrenal Insufficiency

Adrenoleukodystrophy

Immune System Diseases

Autoimmune Diseases

Autoimmune Diseases of the Nervous System

Demyelinating Autoimmune Diseases, CNS

Diffuse Cerebral Sclerosis of Schilder

Immunoproliferative Disorders

Lymphoproliferative Disorders

Animal Diseases

Disease Models, Animal

Primate Diseases

Monkey Diseases

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