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300673
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ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Respiratory Tract Diseases
Respiration Disorders
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsy, Juvenile
Epilepsies, Partial
Epilepsy, Generalized
Epilepsy, Tonic-Clonic
Status Epilepticus
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Rett Syndrome
Neurologic Manifestations
Dyskinesias
Myoclonus
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Rett Syndrome
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypotonia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Incontinentia Pigmenti
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Skin Abnormalities
Incontinentia Pigmenti
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
Skin Diseases, Genetic
Incontinentia Pigmenti
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Incontinentia Pigmenti
Skin Abnormalities
Incontinentia Pigmenti
Skin Diseases, Genetic
Incontinentia Pigmenti
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Disease Attributes
Disease Progression
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Myoclonus
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypotonia
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