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Query gene list
4131
MAP1B
microtubule-associated protein 1B
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Neoplasms
Hamartoma
Tuberous Sclerosis
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Neuroectodermal Tumors, Primitive
Neuroectodermal Tumors, Primitive, Peripheral
Neuroblastoma
Neoplasms, Glandular and Epithelial
Carcinoma
Adenocarcinoma
Carcinoma, Hepatocellular
Neoplasms, Neuroepithelial
Neuroectodermal Tumors, Primitive
Neuroectodermal Tumors, Primitive, Peripheral
Neuroblastoma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Neuroectodermal Tumors, Primitive
Neuroectodermal Tumors, Primitive, Peripheral
Neuroblastoma
Neoplasms by Site
Digestive System Neoplasms
Liver Neoplasms
Carcinoma, Hepatocellular
Neoplasms, Multiple Primary
Tuberous Sclerosis
Neoplastic Syndromes, Hereditary
Tuberous Sclerosis
Digestive System Diseases
Digestive System Neoplasms
Liver Neoplasms
Carcinoma, Hepatocellular
Liver Diseases
Liver Neoplasms
Carcinoma, Hepatocellular
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Injuries
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Cerebrovascular Disorders
Brain Ischemia
Stroke
Dementia
Alzheimer Disease
Epilepsy
Epilepsies, Partial
Seizures
Spinal Cord Diseases
Muscular Atrophy, Spinal
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Nervous System Malformations
Malformations of Cortical Development
Tuberous Sclerosis
Neurocutaneous Syndromes
Tuberous Sclerosis
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Tuberous Sclerosis
Motor Neuron Disease
Muscular Atrophy, Spinal
Tauopathies
Alzheimer Disease
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Seizures
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Peripheral Nervous System Diseases
Polyneuropathies
Trauma, Nervous System
Craniocerebral Trauma
Brain Injuries
Eye Diseases
Retinal Diseases
Vitreoretinopathy, Proliferative
Vitreoretinopathy, Proliferative
Cardiovascular Diseases
Vascular Diseases
Cerebrovascular Disorders
Brain Ischemia
Stroke
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Nervous System Malformations
Malformations of Cortical Development
Tuberous Sclerosis
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Fragile X Syndrome
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Tuberous Sclerosis
Neoplastic Syndromes, Hereditary
Tuberous Sclerosis
Animal Diseases
Disease Models, Animal
Muscular Dystrophy, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Disease Susceptibility
Nerve Degeneration
Retrograde Degeneration
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Seizures
Wounds and Injuries
Craniocerebral Trauma
Brain Injuries
Trauma, Nervous System
Craniocerebral Trauma
Brain Injuries
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