Term Name: amelogenesis imperfecta type 1C
Synonyms: AI1C, amelogenesis imperfecta type IC, autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion, autosomal recessive amelogenesis imperfecta local hypoplastic type
Definition: An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the enamelin gene (ENAM).
Ontology: Human Disease [DOID:0110056]   ( DOID:0110056 )

Relationships
is a type of: amelogenesis imperfecta autosomal recessive disease