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)
OTHER amelogenesis imperfecta hypomaturation type 2A4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ODAPH Amelogenesis imperfecta, type IIA4 614832
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None