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Metadata
ID DOID:0080243
Name amelogenesis imperfecta type 3B
Definition An amelogenesis imperfecta type 3 that is characterized by enamel that is reduced in mineral density and is thin, chipped, and absent in places and that has_material_basis_in heterozygous mutation in the amelotin gene.
https://pubmed.ncbi.nlm.nih.gov/27412008/
Xrefs

OMIM:617607

Parent Relationships

is_a amelogenesis imperfecta type 3

is_a autosomal dominant disease

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