MeSH Treeview
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603365
HIRIP3
HIRA-INTERACTING PROTEIN 3
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Heart Diseases
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge 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
Cardiovascular Abnormalities
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge Syndrome
Lymphatic Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge Syndrome
Endocrine System Diseases
Parathyroid Diseases
Hypoparathyroidism
22q11 Deletion Syndrome
DiGeorge Syndrome
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