Renal hypodysplasia/aplasia 2
MONDO:0014319Any renal agenesis in which the cause of the disease is a mutation in the FGF20 gene.
Also known as: FGF20 renal agenesis (disease), renal agenesis (disease) caused by mutation in FGF20, renal hypodysplasia/aplasia 2, renal hypodysplasia/aplasia type 2, RHDA2
11 clinical trials for this condition and its sub-types.
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Disease
(618)
Kidney disorder
(202)
Hereditary disease
(172)
Urinary system disorder
(62)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Renal agenesis
(1)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)