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 )
Relationships
is a type of:
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
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