MeSH Treeview
Query OMIM entry list
603752
SLC7A4
SOLUTE CARRIER FAMILY 7 (CARIONIC AMINO ACID TRANSPORTER, y+ SYSTEM), MEMBER 4
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Stomatognathic Diseases
Mouth Diseases
Mouth Abnormalities
Velopharyngeal Insufficiency
Pharyngeal Diseases
Velopharyngeal Insufficiency
Stomatognathic System Abnormalities
Mouth Abnormalities
Velopharyngeal Insufficiency
Otorhinolaryngologic Diseases
Pharyngeal Diseases
Velopharyngeal Insufficiency
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Tetralogy of Fallot
Heart Diseases
Heart Defects, Congenital
22q11 Deletion Syndrome
DiGeorge Syndrome
Tetralogy of Fallot
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
Tetralogy of Fallot
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge Syndrome
Lymphatic Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
22q11 Deletion Syndrome
DiGeorge Syndrome
Stomatognathic System Abnormalities
Mouth Abnormalities
Velopharyngeal Insufficiency
Genetic Diseases, Inborn
Chromosome Disorders
22q11 Deletion Syndrome
DiGeorge Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Endocrine System Diseases
Parathyroid Diseases
Hypoparathyroidism
22q11 Deletion Syndrome
DiGeorge Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
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