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renal hypodysplasia/aplasia 2
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any renal agenesis in which the cause of the disease is a mutation in the FGF20 gene.
Uniprot Description A perinatally lethal renal disease encompassing a spectrum of kidney development defects, including renal agenesis, bilateral renal aplasia, hypoplasia, (cystic) dysplasia, and severe obstructive uropathy.
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:615721
UMLS:C3810359
MONDO:0014319
High level summary of knowledge for a disease, including descriptions and datasource references.