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Disease Ontology Browser
lacrimoauriculodentodigital syndrome 1 (DOID:0050331)
Alliance: disease page
Synonyms: Lacrimo-auriculo-dento-digital syndrome 1; LEVY-HOLLISTER SYNDROME
Alt IDs: OMIM:149730
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.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory