Term Name: | amelogenesis imperfecta type 1K |
---|---|
Synonyms: | |
Definition: | An amelogenesis imperfecta characterized by hypoplastic enamel of all teeth that has_material_basis_in heterozygous mutation in the SP6 gene on chromosome 17q21. |
Ontology: | Human Disease [DOID:0060945] ( DOID:0060945 ) |