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Summary Literature (0)
DOID:0081371 - lacrimoauriculodentodigital syndrome 2

Disease Ontology Definition:A LADD syndrome that has_material_basis_in heterozygous mutation in the tyrosine kinase domain of the FGFR3 gene on chromosome 4p16 and that is mainly affecting lacrimal glands and ducts, salivary glands and ducts, ears, teeth, and distal limb segments.

Synonyms: Lacrimo-auriculo-dento-digital syndrome 2,

Xenbase Genes :



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): LADD syndrome (is_a), autosomal dominant disease (is_a)