Disease-gene associations mined from literature

Human genes for prune belly syndrome

Prune belly syndrome [DOID:0060889]

A syndrome that is characterized by megacystis with disorganized detrusor muscle, cryptorchidism, and thin abdominal musculature with overlying lax skin and that has_material_basis_in homozygous mutation in the CHRM3 gene on chromosome 1q43.

Synonyms:  prune belly syndrome,  DOID:0060889,  prune belly disease,  prune belly disorder,  prune belly syndromes ...