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Query OMIM entry list
272200
MSD
MULTIPLE SULFATASE DEFICIENCY
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Neoplasms
Neoplasms by Histologic Type
Histiocytic Disorders, Malignant
Histiocytic Sarcoma
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Multiple Sulfatase Deficiency Disease
Diffuse Cerebral Sclerosis of Schilder
Leukoencephalopathies
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Leukoencephalopathies
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Demyelinating Diseases
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Mucopolysaccharidosis II
Psychomotor Disorders
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Vision Disorders
Blindness
Eye Diseases
Vision Disorders
Blindness
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Diseases
Heart Defects, Congenital
Hemic and Lymphatic Diseases
Lymphatic Diseases
Histiocytosis
Histiocytic Disorders, Malignant
Histiocytic Sarcoma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cardiovascular Abnormalities
Heart Defects, Congenital
Chromosome Disorders
Skin Abnormalities
Ichthyosis
Fetal Diseases
Genetic Diseases, Inborn
Chromosome Disorders
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Mucopolysaccharidosis II
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Mucopolysaccharidosis II
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Multiple Sulfatase Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis II
Mucopolysaccharidosis III
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Multiple Sulfatase Deficiency Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Multiple Sulfatase Deficiency Disease
Mucopolysaccharidoses
Mucopolysaccharidosis II
Mucopolysaccharidosis III
Infant, Newborn, Diseases
Ichthyosis
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis II
Mucopolysaccharidosis III
Skin Diseases
Keratosis
Ichthyosis
Skin Abnormalities
Ichthyosis
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Multiple Sulfatase Deficiency Disease
Lipid Metabolism Disorders
Lipidoses
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Multiple Sulfatase Deficiency Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Multiple Sulfatase Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis II
Mucopolysaccharidosis III
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Multiple Sulfatase Deficiency Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Multiple Sulfatase Deficiency Disease
Mucopolysaccharidoses
Mucopolysaccharidosis II
Mucopolysaccharidosis III
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Vision Disorders
Blindness
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