OBO ID: DOID:0110059
Term Name: X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 Search Ontology:
Synonyms:
  • AIH3
  • amelogenesis imperfecta 3 hypoplastic type
  • amelogenesis imperfecta type IE X-linked 2
  • X-linked enamel hypoplasia
Definition: An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region. https://www.ncbi.nlm.nih.gov/pubmed/1358807
References:
Ontology: Human Disease   ( DOID:0110059 )
Relationships
is a type of:
OTHER X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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