BOR syndrome SNOMEDCT:290006 OMIM:610896 Branchiootorenal syndrome SNOMEDCT:205806009 ICD10:Q87.8 OMIM:113650 NCIt:C98983 Branchio-otorenal dysplasia DOID:14702 Melnick-Fraser syndrome MESH:D019280 UMLS:C0265234 The symptoms and/or signs of branchio-oto-renal syndrome are consistent with underdeveloped (hypoplastic) or absent kidneys with resultant renal insufficiency or renal failure.Ear anomalies include extra openings in front of the ears, extra pieces of skin in front of the ears (preauricular tags), or further malformation or absence of the outer ear (pinna). Malformation or absence of the middle ear is also possible, individuals can have mild to profound hearing loss. People with BOR may also have cysts or fistulae along the sides of their neck. branchiootorenal dysplasia MedDRA:10071135 BOR branchio-oto-renal syndrome Otomandibular dysplasia associated with monogenic syndromes Syndrome or malformation associated with head and neck malformations Genetic renal or urinary tract malformation Genetic branchial arch or oral-acral syndrome Syndromic genetic deafness