has material basis in germline mutation in LONP1 syndromic disease CODAS syndrome https://github.com/monarch-initiative/mondo/issues/4948 https://rarediseases.info.nih.gov/diseases/1418/codas-syndrome https://www.malacards.org/card/codas_syndrome CODAS syndrome cerebrooculodentoauriculoskeletal syndrome MEDGEN:333031 DOID:0111274 GARD:0001418 cerebral, ocular, dental, auricular, and skeletal anomalies syndrome NCIT:C126744 cerebral, ocular, dental, auricular, and skeletal syndrome Codas syndrome is a multiple congenital anomalies syndrome characterized by Cerebral, Ocular, Dental, Auricular and Skeletal anomalies. MESH:C536434 Orphanet:1458 MONDO:0010879 cerebro-oculo-dento-auriculo-skeletal syndrome SCTID:717772000 UMLS:C1838180 OMIM:600373 multiple congenital anomalies/dysmorphic syndrome without intellectual disability spondyloepiphyseal dysplasia