FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term primary failure of tooth eruption ID (Ontology) DOID:0111341 (Human Disease)
Definition A tooth disease characterized by incomplete tooth eruption despite the presence of a clear eruption pathway that has_material_basis_in heterozygous mutation in the PTHR1 gene on chromosome 3p21.31.
Also Known As "dental noneruption" ; "familial posterior openbite malocclusion" ; "nonsyndromic primary failure of eruption" (for all, see Synonyms field below)
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 Genes
 primary failure of tooth eruption       1
 for disease ribbon | primary failure of tooth eruption       1
 model of | primary failure of tooth eruption       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
mouth disease                   |
 |__tooth disease_______________|
                                primary failure of tooth eruption  1 rec.
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Is a autosomal dominant disease
tooth disease
Part of
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Synonyms
  • "dental noneruption" EXACT
    "familial posterior openbite malocclusion" EXACT
    "nonsyndromic primary failure of eruption" EXACT
    "PFE" EXACT OMO:0003012
    "primary retention of teeth" EXACT
    "unerupted second primary molar" EXACT
Secondary IDs
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MESH:C565114
MIM:125350
ORDO:412206
SNOMEDCT_US_2023_03_01:1231153007
UMLS_CUI:C1852222