amelogenesis imperfecta type 3C (DOID:0111722)
Alliance: disease page
Synonyms: AI3C; amelogenesis imperfecta type IIIC; autosomal recessive amelogenesis imperfecta hypocalcification type
Alt IDs: OMIM:618386
Definition: An amelogenesis imperfecta type 3 that is characterized by hypocalcified enamel in both the primary and secondary dentition and that has_material_basis_in homozygous mutation in the RELT gene on chromosome 11q13.