hereditary disease thickened earlobes-conductive deafness syndrome https://www.malacards.org/card/earlobes_thickened_with_conductive_deafness_from_incudostapedial_abnormalities https://www.malacards.org/card/thickened_earlobes_conductive_deafness_syndrome UMLS:C1851896 Escher Hirt syndrome GARD:0002195 Orphanet:2405 MEDGEN:343676 OMIM:128980 Thickened earlobes-conductive deafness syndrome is characterized by microtia with thickened ear lobes, micrognathia and conductive hearing loss due to congenital ossicular anomalies. It has been described in two families. The mode of inheritance is autosomal dominant. Escher-Hirt syndrome SCTID:722476007 MONDO:0007504