OBO ID: DOID:0110052
Term Name: amelogenesis imperfecta type 1B Search Ontology:
Synonyms:
  • AI1B
  • AIH2
  • amelogenesis imperfecta type IB
  • autosomal dominant hypoplastic local amelogenesis imperfecta
  • hereditary localized enamel hypoplasia
Definition: An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the enamelin gene (ENAM) on chromosome 4q13. https://www.ncbi.nlm.nih.gov/pubmed/11487571
References:
Ontology: Human Disease   ( DOID:0110052 )
OTHER amelogenesis imperfecta type 1B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ENAM Amelogenesis imperfecta, type IB
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None