OBO ID: DOID:0080243 |
Term Name: | amelogenesis imperfecta type 3B | Search Ontology: | |
---|---|---|---|
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 ) |
OTHER amelogenesis imperfecta type 3B PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
AMTN | ?Amelogenesis imperfecta, type IIIB |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if
additional information is required.
Oops. Something went wrong. Please try again later.