Search Ontology:
Human Disease

X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2

Term ID
DOID:0110059
Synonyms
  • AIH3
  • amelogenesis imperfecta 3 hypoplastic type
  • amelogenesis imperfecta type IE X-linked 2
  • X-linked enamel hypoplasia
Definition
An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region. https://www.ncbi.nlm.nih.gov/pubmed/1358807
References
Ontology
Human Disease   ( DOID:0110059 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.