MeSH Treeview
Query OMIM entry list
300321
FGS2
FG SYNDROME 2
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Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypotonia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Chromosome Inversion
Disease
Syndrome
Disease Attributes
Facies
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypotonia
Database Center for Life Science
