Search Ontology:
Human Disease

amelogenesis imperfecta type 1J

Term ID
DOID:0080953
Synonyms
  • Amelogenesis imperfecta, type IJ
Definition
An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the ACPT on chromosome 19q13. https://pubmed.ncbi.nlm.nih.gov/27843125/
References
Ontology
Human Disease   ( DOID:0080953 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models