Term Name: amelogenesis imperfecta hypomaturation type 2A3
Synonyms: AI2A3, amelogenesis imperfecta hypomaturation type IIA3, amelogenesis imperfecta type IIA3
Definition: An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene.
Ontology: Human Disease [DOID:0110061]   ( DOID:0110061 )

Relationships
is a type of: amelogenesis imperfecta autosomal recessive disease