FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term amelogenesis imperfecta type 4 ID (Ontology) DOID:0110053 (Human Disease)
Definition An amelogenesis imperfecta which can has_material_basis_in mutation in the DLX3 gene.
Also Known As "AI4" ; "AIHHT" ; "amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism"
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DO.org
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 Genes
 amelogenesis imperfecta type 4       1
 for disease ribbon | amelogenesis imperfecta type 4       1
 model of | amelogenesis imperfecta type 4       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
dental enamel hypoplasia        |
 |__amelogenesis imperfecta_____|
                                amelogenesis imperfecta type 4  1 rec.
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Is a autosomal dominant disease
amelogenesis imperfecta
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Synonyms
  • "AI4" EXACT OMO:0003012
    "AIHHT" EXACT OMO:0003012
    "amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism" EXACT
Secondary IDs
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ICD10CM:K00.5
MIM:104510