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309900
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MUCOPOLYSACCHARIDOSIS TYPE II
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Musculoskeletal Diseases
Joint Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Respiratory Tract Diseases
Respiration Disorders
Respiratory Insufficiency
Airway Obstruction
Tracheal Diseases
Tracheal Stenosis
Otorhinolaryngologic Diseases
Ear Diseases
Otitis
Otitis Media
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Seizures
Spinal Cord Diseases
Spinal Cord Compression
Cranial Nerve Diseases
Optic Nerve Diseases
Papilledema
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Mucopolysaccharidosis II
Seizures
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Optic Nerve Diseases
Papilledema
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Eye Diseases, Hereditary
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Mucopolysaccharidosis II
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Fragile X Syndrome
Mucopolysaccharidosis II
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Lysosomal Storage Diseases
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Muscular Dystrophies
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Skin Diseases
Pigmentation Disorders
Hyperpigmentation
Skin Diseases, Papulosquamous
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
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosomal Instability
Chromosome Fragility
Chromosome Inversion
Sex Chromosome Aberrations
Translocation, Genetic
Disease Attributes
Chronic Disease
Diseases in Twins
Recurrence
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Seizures
Wounds and Injuries
Spinal Cord Injuries
Spinal Cord Compression
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