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Query OMIM entry list
606232
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CHROMOSOME 22q13.3 DELETION SYNDROME
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Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Language Development Disorders
Intellectual Disability
Mental Retardation, X-Linked
Neuromuscular Manifestations
Muscle Hypotonia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Nutritional and Metabolic Diseases
Nutrition Disorders
Overnutrition
Obesity
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Ring Chromosomes
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Facies
Recurrence
Growth Disorders
Signs and Symptoms
Body Weight
Overweight
Obesity
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Language Development Disorders
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypotonia
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