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 )

Relationships
is a type of: amelogenesis imperfecta