MeSH Treeview
Query OMIM entry list
137350
GSN
GELSOLIN
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High-scoring List
Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Myeloid
Neoplasms by Site
Urogenital Neoplasms
Genital Neoplasms, Male
Prostatic Neoplasms
Digestive System Diseases
Pancreatic Diseases
Cystic Fibrosis
Stomatognathic Diseases
Mouth Diseases
Facial Paralysis
Respiratory Tract Diseases
Lung Diseases
Cystic Fibrosis
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Dystonia Musculorum Deformans
Movement Disorders
Dystonic Disorders
Dystonia Musculorum Deformans
Demyelinating Diseases
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Dystonia Musculorum Deformans
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Neurologic Manifestations
Paralysis
Facial Paralysis
Neuromuscular Diseases
Peripheral Nervous System Diseases
Amyloid Neuropathies
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Eye Diseases
Corneal Diseases
Corneal Dystrophies, Hereditary
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Male Urogenital Diseases
Genital Diseases, Male
Genital Neoplasms, Male
Prostatic Neoplasms
Prostatic Diseases
Prostatic Neoplasms
Urogenital Neoplasms
Genital Neoplasms, Male
Prostatic Neoplasms
Urologic Diseases
Kidney Diseases
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Genetic Diseases, Inborn
Cystic Fibrosis
Eye Diseases, Hereditary
Corneal Dystrophies, Hereditary
Heredodegenerative Disorders, Nervous System
Dystonia Musculorum Deformans
Hereditary Sensory and Motor Neuropathy
Hereditary Sensory and Autonomic Neuropathies
Metabolism, Inborn Errors
Amyloidosis, Familial
Infant, Newborn, Diseases
Cystic Fibrosis
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amyloidosis, Familial
Proteostasis Deficiencies
Amyloidosis
Amyloid Neuropathies
Amyloidosis, Familial
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Inflammation
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Paralysis
Facial Paralysis
Skin Manifestations
Database Center for Life Science
