FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term lacrimoauriculodentodigital syndrome 3 ID (Ontology) DOID:0081372 (Human Disease)
Definition A LADD syndrome that is characterized by aplasia, atresia or hypoplasia of the lacrimal and salivary systems, cup-shaped ears, hearing loss, and dental and digital anomalies and that has_material_basis_in heterozygous mutation in the FGF10 gene on chromosome 5p12.
Also Known As "Lacrimo-auriculo-dento-digital syndrome 3"
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 Genes
 lacrimoauriculodentodigital syndrome 3       1
 for disease ribbon | lacrimoauriculodentodigital syndrome 3       1
 model of | lacrimoauriculodentodigital syndrome 3       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
syndrome                        |
 |__LADD syndrome_______________|
                                lacrimoauriculodentodigital syndrome 3  1 rec.
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Is a autosomal dominant disease
LADD syndrome
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Synonyms
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Secondary IDs
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MIM:620193