National Library of Medicine - Medical Subject Headings

2012 MeSH

MeSH Descriptor Data

Return to Entry Page

Standard View. Go to Concept ViewGo to Expanded Concept View

DiGeorge Syndrome
MeSH HeadingDiGeorge Syndrome
Tree NumberC05.660.207.103.500
Tree NumberC14.240.400.021.500
Tree NumberC14.280.400.044.500
Tree NumberC15.604.451.249.500
Tree NumberC16.131.077.019.500
Tree NumberC16.131.240.400.021.500
Tree NumberC16.131.260.019.500
Tree NumberC16.131.482.249.500
Tree NumberC16.131.621.207.103.500
Tree NumberC16.320.180.019.500
Tree NumberC19.642.482.500.500
Scope NoteCongenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies.
Entry TermConotruncal Anomaly Face Syndrome
Entry TermDiGeorge Anomaly
Entry TermDiGeorge Sequence
Entry TermFamilial Third and Fourth Pharyngeal Pouch Syndrome
Entry TermHypoplasia of Thymus and Parathyroids
Entry TermPharyngeal Pouch Syndrome
Entry TermThird and Fourth Pharyngeal Pouch Syndrome
Entry TermThymic Aplasia Syndrome
Entry TermVelo-Cardio-Facial Syndrome
Entry TermVelocardiofacial Syndrome
Allowable QualifiersBL CF CI CL CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
Previous Indexing Parathyroid Glands (1966-1976)
Previous Indexing Thymus Gland (1966-1976)
History Note91(77); was see under IMMUNOLOGIC DEFICIENCY SYNDROMES 1977-90
Date of Entry19760416
Unique IDD004062


MeSH Tree Structures

 
Musculoskeletal Diseases [C05]
   Musculoskeletal Abnormalities [C05.660]
      Craniofacial Abnormalities [C05.660.207]
         22q11 Deletion Syndrome [C05.660.207.103]
Arrow pointing to current tree nodeDiGeorge Syndrome [C05.660.207.103.500]

 
Cardiovascular Diseases [C14]
   Cardiovascular Abnormalities [C14.240]
      Heart Defects, Congenital [C14.240.400]
         22q11 Deletion Syndrome [C14.240.400.021]
Arrow pointing to current tree nodeDiGeorge Syndrome [C14.240.400.021.500]

 
Cardiovascular Diseases [C14]
   Heart Diseases [C14.280]
      Heart Defects, Congenital [C14.280.400]
         22q11 Deletion Syndrome [C14.280.400.044]
Arrow pointing to current tree nodeDiGeorge Syndrome [C14.280.400.044.500]

 
Hemic and Lymphatic Diseases [C15]
   Lymphatic Diseases [C15.604]
      Lymphatic Abnormalities [C15.604.451]
         22q11 Deletion Syndrome [C15.604.451.249]
Arrow pointing to current tree nodeDiGeorge Syndrome [C15.604.451.249.500]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Congenital Abnormalities [C16.131]
      Abnormalities, Multiple [C16.131.077]
         22q11 Deletion Syndrome [C16.131.077.019]
Arrow pointing to current tree nodeDiGeorge Syndrome [C16.131.077.019.500]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Congenital Abnormalities [C16.131]
      Cardiovascular Abnormalities [C16.131.240]
         Heart Defects, Congenital [C16.131.240.400]
            22q11 Deletion Syndrome [C16.131.240.400.021]
Arrow pointing to current tree nodeDiGeorge Syndrome [C16.131.240.400.021.500]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Congenital Abnormalities [C16.131]
      Chromosome Disorders [C16.131.260]
         22q11 Deletion Syndrome [C16.131.260.019]
Arrow pointing to current tree nodeDiGeorge Syndrome [C16.131.260.019.500]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Congenital Abnormalities [C16.131]
      Lymphatic Abnormalities [C16.131.482]
         22q11 Deletion Syndrome [C16.131.482.249]
Arrow pointing to current tree nodeDiGeorge Syndrome [C16.131.482.249.500]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Congenital Abnormalities [C16.131]
      Musculoskeletal Abnormalities [C16.131.621]
         Craniofacial Abnormalities [C16.131.621.207]
            22q11 Deletion Syndrome [C16.131.621.207.103]
Arrow pointing to current tree nodeDiGeorge Syndrome [C16.131.621.207.103.500]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Chromosome Disorders [C16.320.180]
         22q11 Deletion Syndrome [C16.320.180.019]
Arrow pointing to current tree nodeDiGeorge Syndrome [C16.320.180.019.500]

 
Endocrine System Diseases [C19]
   Parathyroid Diseases [C19.642]
      Hypoparathyroidism [C19.642.482]
         22q11 Deletion Syndrome [C19.642.482.500]
Arrow pointing to current tree nodeDiGeorge Syndrome [C19.642.482.500.500]

Return to Entry Page Link to NLM Cataloging Classification