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congenital hydronephrosis
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Congenital hydronephrosis is a renal urinary disease characterized by distension and dilation of the renal pelvis and calyces secondary to various congenital obstructive malformations of the kidneys and urinary tract that can evolve to renal atrophy.
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.
COHD:4037874
ICD10:Q62.0
NCIT:C102979
Orphanet:2190
SCTID:16297002
UMLS:C0266316
MONDO:0007741
High level summary of knowledge for a disease, including descriptions and datasource references.