has material basis in germline mutation in DSPP hereditary disease dentinogenesis imperfecta type 3 https://rarediseases.info.nih.gov/diseases/10144/dentinogenesis-imperfecta-type-3 https://www.malacards.org/card/dentinogenesis_imperfecta_shields_type_iii OMIM:125500 Dentinogenesis imperfecta type 3 (DGI-3) is a rare, severe form of dentinogenesis imperfecta (DGI) characterized by opalescent primary and permanent teeth, marked attrition, large pulp chambers, multiple pulp exposure and shell teeth radiographically (i.e. teeth which appear hollow due to dentin hypotrophy). dentinogenesis imperfecta, Shields type 3 MONDO:0007442 dentinogenesis imperfecta, Shields type III MESH:C538216 NORD:1043 Dentinogenesis Imperfecta Type III MEDGEN:97995 UMLS:C0399378 ICD9:520.5 dentinogenesis imperfecta type III DGI-III icd11.foundation:518257495 brandywine type dentinogenesis imperfecta GARD:0010144 Orphanet:166265 SCTID:234970006 dentinogenesis imperfecta Shields type 3 dentinogenesis imperfecta