disease has basis in dysfunction of GATA3 syndrome caused by partial chromosomal deletion hypoparathyroidism-deafness-renal disease syndrome Barakat syndrome DOID:0060878 GARD:0002911 HDR HDR syndrome ICD10:Q87.8 MESH:C537907 MONDO:0007797 NCIT:C130983 OMIM:146255 Orphanet:2237 SCTID:724282009 The HDR syndrome is an inherited condition consisting of hypoparathyroidism, sensorineural deafness and renal disease. UMLS:C1840333 hypoparathyroidism, deafness, and renal anomalies syndrome hypoparathyroidism, sensorineural deafness, and renal disease hypoparathyroidism, sensorineural deafness, and renal dysplasia hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome nephrosis, nerve deafness, and hypoparathyroidism syndromic urogenital tract malformation syndrome with hypoparathyroidism partial deletion of the short arm of chromosome 10 syndromic genetic deafness syndromic renal or urinary tract malformation