OBO ID: DOID:0110062
Term Name: amelogenesis imperfecta hypomaturation type 2A4 Search Ontology:
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 amelogenesis imperfecta hypomaturation type 2A4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ODAPH Amelogenesis imperfecta, type IIA4
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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.