Disease & disorder
congenital anomalies of kidney and urinary tract 2
MONDO:0027676
Any congenital anomaly of kidney and urinary tract in which the cause of the disease is a mutation in the TBX18 gene.
Outbreak surveillance
Global reported eventsExplore recent public health notices potentially related to congenital anomalies of kidney and urinary tract 2. Results are keyword matches, not yet verified disease-to-outbreak relationships.
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Background context
congenital anomalies of kidney and urinary tract 2
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.Drugs being studied
Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.