MeSH Treeview
Query OMIM entry list
610543
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CHROMOSOME 16p13.3 DELETION SYNDROME
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Rubinstein-Taybi Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Rubinstein-Taybi Syndrome
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Rubinstein-Taybi Syndrome
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Hypoplastic Left Heart Syndrome
Heart Diseases
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Hypoplastic Left Heart Syndrome
Hemic and Lymphatic Diseases
Lymphatic Diseases
Lymphatic Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
22q11 Deletion Syndrome
DiGeorge Syndrome
Rubinstein-Taybi Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Hypoplastic Left Heart Syndrome
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge Syndrome
Rubinstein-Taybi Syndrome
Lymphatic Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Rubinstein-Taybi Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge Syndrome
Rubinstein-Taybi Syndrome
Endocrine System Diseases
Parathyroid Diseases
Hypoparathyroidism
22q11 Deletion Syndrome
DiGeorge Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
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