MeSH Treeview
Query OMIM entry list
300486
-
MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE
→
High-scoring List
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Epilepsy
Epilepsies, Myoclonic
Nervous System Malformations
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Facial Asymmetry
Pathologic Processes
Chromosome Aberrations
Chromosome Breakage
Translocation, Genetic
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Database Center for Life Science