Search Ontology:
Human Disease

amelogenesis imperfecta type 1H

Term ID
DOID:0110064
Synonyms
  • AI1H
  • amelogenesis imperfecta type IH
Definition
An amelogenesis imperfecta that has_material_basis_in homozygous or compound heterozygous mutation in the integrin beta-6 gene (ITGB6) on chromosome 2q24. (2)
References
Ontology
Human Disease   ( DOID:0110064 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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