Search Ontology:
Human Disease

amelogenesis imperfecta hypomaturation type 2A5

Term ID
DOID:0110063
Synonyms
  • AI2A5
  • amelogenesis imperfecta hypomaturation type IIA5
  • amelogenesis imperfecta type IIA5
Definition
An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the SLC24A4 gene on chromosome 14q32. https://www.ncbi.nlm.nih.gov/pubmed/23375655
References
Ontology
Human Disease   ( DOID:0110063 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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