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Summary Literature (0)
DOID:0050331 - LADD syndrome

Disease Ontology Definition:An autosomal dominant disease that is characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes.

Synonyms: LEVY-HOLLISTER SYNDROME, lacrimoauriculodentodigital syndrome,

Echinobase Genes : fgfr3

MIM:149730 - lacrimoauriculodentodigital syndrome; ladd

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

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