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Disease Ontology Browser
aplasia of lacrimal and salivary glands (DOID:0111549)
Alliance: disease page
Synonyms: ALSG; congenital absence of lacrimal puncta and salivary glands
Alt IDs: OMIM:180920, ICD9CM:750.21, MESH:C562407, ORDO:86815, UMLS_CUI:C0158667
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.

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