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308840
L1CAM
L1 CELL ADHESION MOLECULE
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Neoplasms
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
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
Musculoskeletal Diseases
Muscular Diseases
Muscle Spasticity
Digestive System Diseases
Digestive System Abnormalities
Hirschsprung Disease
Gastrointestinal Diseases
Intestinal Diseases
Colonic Diseases
Megacolon
Hirschsprung Disease
Intestinal Obstruction
Ileus
Intestinal Pseudo-Obstruction
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Hydrocephalus
Intracranial Hypertension
Hydrocephalus
Movement Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Aphasia
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Paralysis
Paraplegia
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Digestive System Abnormalities
Hirschsprung Disease
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Fetal Diseases
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
Hereditary Sensory and Motor Neuropathy
Spastic Paraplegia, Hereditary
Mental Retardation, X-Linked
Fragile X Syndrome
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Constriction, Pathologic
Pathologic Processes
Chromosome Aberrations
Sex Chromosome Aberrations
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Aphasia
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Paralysis
Paraplegia
Wounds and Injuries
Dislocations
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