Human genes for Perlman syndrome
Perlman syndrome [DOID:0060476]
A syndrome characterized by polyhydramnios with neonatal macrosomia, nephromegaly, distinctive facial appearance, renal dysplasia, nephroblastomatosis, and predisposition to Wilms tumor. It shows similarities to Beckwith-Wiedemann syndrome.
Synonyms: Perlman syndrome, DOID:0060476, Perlman disease, Perlman disorder, Perlman syndromes ...