Hinman syndrome (HS)

Voiding dysfunction of the bladder of neuropsychological origin that is characterized by functional bladder outlet obstruction in the absence of neurologic deficits.

Denys-Drash syndrome (DDS)

Rare genetic condition caused by mutations in WT-1 (11p13), a tumor-suppressor gene involved in gonadal development

Sinding-Larsen-Johansson (SLJ) syndrome

Syndrome characterized by periostitis of inferior pole of patella.

Mucopolysaccharidosis type I (MPS I)

Rare lysosomal storage disorder due to deficiency of lysosomal enzyme α1-iduronidase resulting in progressive accumulation of glycosaminoglycans (GAG) within lysosomes, leading to multiorgan dysfunction and damage.