Term Name: amelogenesis imperfecta hypomaturation type 2A5
Synonyms: AI2A5, amelogenesis imperfecta hypomaturation type IIA5, amelogenesis imperfecta type IIA5
Definition: An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the SLC24A4 gene on chromosome 14q32.
Ontology: Human Disease [DOID:0110063]   ( DOID:0110063 )

Relationships
is a type of: amelogenesis imperfecta autosomal recessive disease