OBO ID: DOID:0110061
Term Name: amelogenesis imperfecta hypomaturation type 2A3 Search Ontology:
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 amelogenesis imperfecta hypomaturation type 2A3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WDR72 Amelogenesis imperfecta, type IIA3
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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