About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory