disease arises from structure disease arises from alteration in structure Xq22.3 (Human) kidney disorder X-linked diffuse leiomyomatosis-Alport syndrome https://github.com/monarch-initiative/mondo/issues/3664 https://www.malacards.org/card/leiomyomatosis_diffuse_with_alport_syndrome https://www.malacards.org/card/x_linked_diffuse_leiomyomatosis_alport_syndrome_2 UMLS:C1839884 ATS-DL MEDGEN:333429 chromosome Xq22.3 centromeric deletion syndrome diffuse leiomyomatosis in Alport syndrome Orphanet:1018 A rare renal disease characterized by the association of X-linked Alport syndrome (glomerular nephropathy, sensorineural deafness and ocular anomalies) and benign proliferation of visceral smooth muscle cells along the gastrointestinal, respiratory, and female genital tracts and clinically manifests with dysphagia, dyspnea, cough, stridor, postprandial vomiting, retrosternal or epigastric pain, recurrent pneumonia, and clitoral hypertrophy in females. Xq22.3 microdeletion syndrome OMIM:308940 Alport syndrome with diffuse leiomyomatosis Alport syndrome and diffuse leiomyomatosis DL-ATS MONDO:0010641 MESH:C537113 leiomyomatosis, diffuse, with Alport syndrome leiomyomatosis, esophageal and vulval, with nephropathy GARD:0002432 partial deletion of the long arm of chromosome X