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314900
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XM SYSTEM
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Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Mucopolysaccharidosis II
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Hemophilia A
Hemophilia B
Coagulation Protein Disorders
Hemophilia A
Hemophilia B
Hemorrhagic Disorders
Hemophilia A
Hemophilia B
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hemophilia A
Hemophilia B
Genetic Diseases, X-Linked
Hemophilia B
Mental Retardation, X-Linked
Mucopolysaccharidosis II
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Mucopolysaccharidosis II
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Lysosomal Storage Diseases
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Lysosomal Storage Diseases
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
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