Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 796
Gene Symbol: CALCA
CALCA
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.030 Biomarker BEFREE To test the hypothesis that mutations in the calcitonin/CGRP gene might be responsible for the reduced calcitonin levels, we examined the calcitonin/CGRP gene structure in Williams syndrome children. 1867260

1991
Entrez Id: 796
Gene Symbol: CALCA
CALCA
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.030 Biomarker BEFREE The calcitonin-CGRP gene in the infantile hypercalcaemia/Williams-Beuren syndrome. 2486208

1989
Entrez Id: 796
Gene Symbol: CALCA
CALCA
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.030 Biomarker BEFREE It has been suggested that a defect in calcitonin function may play a role in Williams syndrome. 3164411

1988