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PedAM

Pediatric Disease Annotations & Medicines




Disease gonadal dysgenesis
Phenotype C0017668|focal segmental glomerulosclerosis
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PubMedID- 22815844 As the patient had 46,xy gonadal dysgenesis together with renal failure (focal segmental glomerulosclerosis), and gb with dysgerminoma, without wilm’s tumor, all pointing to fs, the wt1 gene was analyzed.

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