Term Name: amelogenesis imperfecta hypomaturation type 2A4
Synonyms: AI2A4, amelogenesis imperfecta hypomaturation type IIA4, amelogenesis imperfecta type IIA4
Definition: An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21.
Ontology: Human Disease [DOID:0110062]   ( DOID:0110062 )

Relationships
is a type of: amelogenesis imperfecta autosomal recessive disease