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uniparental disomy
Disease Summary
Associated Targets (3)
Tchem
1
Tbio
1
Tdark
1
Mondo Description A condition characterized by the inheritance of a chromosome pair from one parent and no chromosomal copies from the other parent. It results in developmental abnormalities or rare recessive disorders.
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.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
NCIT:C85215
MONDO:0700086
High level summary of knowledge for a disease, including descriptions and datasource references.