Search Ontology:
Human Disease
amelogenesis imperfecta type 3B
- Term ID
- DOID:0080243
- Synonyms
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- 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 )
- is a type of
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Genes Involved
Zebrafish Models