Search Ontology:
Human Disease

amelogenesis imperfecta type 1C

Term ID
DOID:0110056
Synonyms
  • AI1C
  • amelogenesis imperfecta type IC
  • autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion
  • autosomal recessive amelogenesis imperfecta local hypoplastic type
Definition
An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the enamelin gene (ENAM). https://www.ncbi.nlm.nih.gov/pubmed/14684688
References
Ontology
Human Disease   ( DOID:0110056 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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