has material basis in germline mutation in CHRM3 syndromic disease prune belly syndrome https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/prune_belly_syndrome MESH:D011535 PBS OMIM:100100 Obrisnksy syndrome Obrinsky syndrome Orphanet:2970 MEDGEN:18718 ICD10CM:Q79.4 syndrome of agenesis of abdominal muscles eagle-Barrett syndrome eagle-Barret syndrome MedDRA:10051025 prune belly syndrome GARD:0007479 SCTID:5187006 Prune belly syndrome is a rare congenital disorder, belonging to the group of fetal lower urinary tract obstructions (LUTO), involving variable dilation of the lower urinary tract in association with partial or complete absence of the lateral and inferior abdominal wall musculature and in males bilateral non-palpable undescended testes. triad syndrome ICD9:756.71 abdominal muscles, absence of, with urinary tract Abnormality and cryptorchidism MONDO:0007032 UMLS:C0033770 abdominal muscle deficiency syndrome icd11.foundation:1393408621 NCIT:C85033 NORD:1623 NANDO:2200185 DOID:0060889 fetal lower urinary tract obstruction inherited kidney disorder