OBO ID: DOID:0110058
Term Name: amelogenesis imperfecta type 1E Search Ontology:
Synonyms:
  • AIH1
  • amelogenesis imperfecta hypomaturationtype with snow-capped teeth
  • amelogenesis imperfecta type IE
  • X-linked amelogenesis imperfecta 1
  • X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1
  • X-linked enamel hypoplasia
Definition: An amelogenesis imperfecta that has_material_basis_in X-linked dominant mutation in the gene encoding amelogenin (AMELX). (2)
References:
Ontology: Human Disease   ( DOID:0110058 )
Relationships
is a type of:
OTHER amelogenesis imperfecta type 1E PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
AMELX Amelogenesis imperfecta, type 1E
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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