TBX1, T-box transcription factor 1, 6899

N. diseases: 417; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia
0.140 GeneticVariation phenotype BEFREE TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia. 24637876 2014
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia
0.140 GeneticVariation phenotype BEFREE The authors pointed out the necessity of DGS suspicion in all patient presenting with heart defects, facial abnormalities (associated or not with hypocalcemia), and immunological disorders because although frequency of DGS is high, few patients with a confirmed diagnosis are followed up. 21049214 2010
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia
0.140 Biomarker phenotype BEFREE CATCH 22 is an acronym for cardiac defect, abnormal facies, thymic hypoplasia or aplasia and T-cell deficiency, cleft palate, hypoparathyroidism, and hypocalcemia. 9099830 1997
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia
0.140 GeneticVariation phenotype BEFREE The CATCH 22 acronym outlines the main clinical features of 22q11.2 deletions (cardiac defects, abnormal facies, thymic hypoplasia, cleft palate and hypocalcemia), usually found in DiGeorge (DGS) and velo-cardio-facial (VCFS) syndromes. 9063746 1997
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia
0.140 Biomarker phenotype HPO