Term Name: amelogenesis imperfecta type 1A
Synonyms: AI1A, amelogenesis imperfecta hypoplastic type IA, amelogenesis imperfecta type IA
Definition: An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the beta-3 laminin gene (LAMB3) on chromosome 1q32.
Ontology: Human Disease [DOID:0110054]   ( DOID:0110054 )

Relationships
is a type of: amelogenesis imperfecta autosomal dominant disease