OBO ID: DOID:0111549
Term Name: aplasia of lacrimal and salivary glands Search Ontology:
Synonyms:
  • ALSG
  • congenital absence of lacrimal puncta and salivary glands
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. https://www.ncbi.nlm.nih.gov/pubmed/15654336
References:
Ontology: Human Disease   ( DOID:0111549 )
Relationships
is a type of:
OTHER aplasia of lacrimal and salivary glands PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FGF10 Aplasia of lacrimal and salivary glands 180920
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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