has material basis in germline mutation in FGF3 hereditary disease deafness with labyrinthine aplasia, microtia, and microdontia https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/deafness_congenital_with_inner_ear_agenesis_microtia_and_microdontia_2 OMIM:610706 deafness congenital with inner ear agenesis microtia and microdontia GARD:0010707 microdontia-type I microtia-deafness syndrome MESH:C565195 MEDGEN:342803 deafness with labyrinthine aplasia, microtia, and microdontia deafness with labyrinthine aplasia microtia and microdontia (LAMM) MONDO:0012541 ICD9:759.89 LAMM syndrome Deafness with labyrinthine aplasia, microtia, and microdontia (LAMM) is a genetic transmission deafness syndrome. deafness, congenital with inner ear agenesis, microtia, and microdontia UMLS:C1853144 congenital deafness with inner ear agenesis microtia and microdontia Orphanet:90024 SCTID:702360007