Search Ontology:
Human Disease

amelogenesis imperfecta hypomaturation type 2A4

Term ID
DOID:0110062
Synonyms
  • AI2A4
  • amelogenesis imperfecta hypomaturation type IIA4
  • amelogenesis imperfecta type IIA4
Definition
An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21. https://www.ncbi.nlm.nih.gov/pubmed/22901946
References
Ontology
Human Disease   ( DOID:0110062 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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