Search Ontology:
Human Disease

amelogenesis imperfecta type 1E

Term ID
DOID:0110058
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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