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Summary Literature (0)
DOID:0111549 - aplasia of lacrimal and salivary glands

Disease Ontology Definition:A syndrome characterized by irritable eyes, epiphora, xerostomia, variable aplasia or hypoplasia of the lacrimal, parotid, submandibular, and sublingual glands, and absence of the lacrimal puncta that has_material_basis_in heterozygous mutation in the FGF10 gene on chromosome 5p12.

Synonyms: ALSG, congenital absence of lacrimal puncta and salivary glands

Xenbase Genes : fgf10


MIM:
MIM:180920 - APLASIA OF LACRIMAL AND SALIVARY GLANDS; ALSG

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), syndrome (is_a)