has material basis in lacrimoauriculodentodigital syndrome 1 MIM:149730 disease_ontology 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. DOID:0050331 LEVY-HOLLISTER SYNDROME Lacrimo-auriculo-dento-digital syndrome 1 OMIM mapping confirmed by DO. [SN]. autosomal dominant disease LADD syndrome autosomal dominant inheritance