FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term lacrimoauriculodentodigital syndrome 1 ID (Ontology) DOID:0050331 (Human Disease)
Definition A syndrome that has_material_basis_in heterozygous mutation in the tyrosine kinase domain of the FGFR2 gene on chromosome 10q26 and that is characterized by autosomal dominant inheritance of abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes.
Also Known As "Lacrimo-auriculo-dento-digital syndrome 1" ; "LEVY-HOLLISTER SYNDROME"
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 Genes
 lacrimoauriculodentodigital syndrome 1       2
 for disease ribbon | lacrimoauriculodentodigital syndrome 1       2
 model of | lacrimoauriculodentodigital syndrome 1       2
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autosomal genetic disease
 |__autosomal dominant disease__
syndrome                        |
 |__LADD syndrome_______________|
                                lacrimoauriculodentodigital syndrome 1  2 rec.
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Is a autosomal dominant disease
LADD syndrome
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Synonyms
  • "Lacrimo-auriculo-dento-digital syndrome 1" EXACT
    "LEVY-HOLLISTER SYNDROME" EXACT
Secondary IDs
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MIM:149730