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Human Disease

amelogenesis imperfecta type 3B

Term ID
DOID:0080243
Synonyms
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/
References
Ontology
Human Disease   ( DOID:0080243 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models