Search Ontology:
Human Disease

X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2

Term ID
DOID:0110059
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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