Search Ontology:
Human Disease

amelogenesis imperfecta hypomaturation type 2A3

Term ID
DOID:0110061
Synonyms
  • AI2A3
  • amelogenesis imperfecta hypomaturation type IIA3
  • amelogenesis imperfecta type IIA3
Definition
An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene. https://www.ncbi.nlm.nih.gov/pubmed/19853237
References
Ontology
Human Disease   ( DOID:0110061 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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