MeSH Treeview
Query OMIM entry list
308350
-
INFANTILE SPASM SYNDROME, X-LINKED
→
High-scoring List
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Spinocerebellar Degenerations
Epilepsy
Epilepsy, Generalized
Spasms, Infantile
Seizures
Status Epilepticus
Headache Disorders
Headache Disorders, Primary
Migraine Disorders
Movement Disorders
Dystonic Disorders
Spinal Cord Diseases
Spinocerebellar Degenerations
Cranial Nerve Diseases
Optic Nerve Diseases
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Rett Syndrome
Spinocerebellar Degenerations
Neurologic Manifestations
Neurobehavioral Manifestations
Consciousness Disorders
Unconsciousness
Syncope
Intellectual Disability
Mental Retardation, X-Linked
Rett Syndrome
Neuromuscular Manifestations
Muscle Hypotonia
Seizures
Eye Diseases
Ocular Hypertension
Optic Nerve Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Rett Syndrome
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Rett Syndrome
Rett Syndrome
Spinocerebellar Degenerations
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Chromosome Aberrations
Sex Chromosome Aberrations
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Consciousness Disorders
Unconsciousness
Syncope
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypotonia
Seizures
Database Center for Life Science
