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105400
ALS1
AMYOTROPHIC LATERAL SCLEROSIS 1
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Virus Diseases
Central Nervous System Viral Diseases
Encephalitis
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Connective and Soft Tissue
Neoplasms, Connective Tissue
Neoplasms, Bone Tissue
Osteochondroma
Osteochondromatosis
Exostoses, Multiple Hereditary
Neoplastic Syndromes, Hereditary
Exostoses, Multiple Hereditary
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Osteochondroma
Osteochondromatosis
Exostoses, Multiple Hereditary
Hyperostosis
Exostoses
Exostoses, Multiple Hereditary
Joint Diseases
Hip Dislocation, Congenital
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Hip Dislocation, Congenital
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Dementia
Alzheimer Disease
Creutzfeldt-Jakob Syndrome
Huntington Disease
Encephalitis
Central Nervous System Infections
Central Nervous System Viral Diseases
Encephalitis
Encephalitis
Prion Diseases
Creutzfeldt-Jakob Syndrome
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Spinal Cord Diseases
Amyotrophic Lateral Sclerosis
Muscular Atrophy, Spinal
Demyelinating Diseases
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Malformations of Cortical Development
Microcephaly
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Huntington Disease
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Muscular Atrophy, Spinal
Parkinson Disease
Tauopathies
Alzheimer Disease
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Paralysis
Neuromuscular Diseases
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Eye Diseases
Lens Diseases
Cataract
Cardiovascular Diseases
Heart Diseases
Myocardial Ischemia
Coronary Disease
Vascular Diseases
Angioedema
Hemostatic Disorders
Telangiectasia, Hereditary Hemorrhagic
Myocardial Ischemia
Coronary Disease
Telangiectasis
Telangiectasia, Hereditary Hemorrhagic
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Hemophilia A
Coagulation Protein Disorders
Hemophilia A
Hemorrhagic Disorders
Hemophilia A
Hemostatic Disorders
Telangiectasia, Hereditary Hemorrhagic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Cardiovascular Abnormalities
Vascular Malformations
Telangiectasia, Hereditary Hemorrhagic
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Hip Dislocation, Congenital
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Malformations of Cortical Development
Microcephaly
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hemophilia A
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Huntington Disease
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Alkaptonuria
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Lysosomal Storage Diseases
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Muscular Dystrophies
Neoplastic Syndromes, Hereditary
Exostoses, Multiple Hereditary
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Skin Diseases
Skin Diseases, Vascular
Urticaria
Angioedema
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Alkaptonuria
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Lysosomal Storage Diseases
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Proteostasis Deficiencies
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Nutrition Disorders
Infant Nutrition Disorders
Malnutrition
Deficiency Diseases
Immune System Diseases
Hypersensitivity
Hypersensitivity, Immediate
Urticaria
Angioedema
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Disease
Syndrome
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Anticipation, Genetic
Nerve Degeneration
Signs and Symptoms
Body Weight
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Paralysis
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