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tooth agenesis, selective, 7
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any tooth agenesis in which the cause of the disease is a mutation in the LRP6 gene.
Uniprot Description An autosomal dominant form of selective tooth agenesis, a common anomaly characterized by the congenital absence of one or more teeth. Selective tooth agenesis without associated systemic disorders has sometimes been divided into 2 types: oligodontia, defined as agenesis of 6 or more permanent teeth, and hypodontia, defined as agenesis of less than 6 teeth. The number in both cases does not include absence of third molars (wisdom teeth).
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:616724
UMLS:C4225231
MONDO:0014749
High level summary of knowledge for a disease, including descriptions and datasource references.