intermediate anorectal malformation https://github.com/monarch-initiative/mondo/issues/6876 UMLS:C4518340 MONDO:0015732 icd11.foundation:1224425167 Intermediate anorectal malformation is a rare, genetic, non-syndromic subtype of anorectal malformation, resulting from a developmental defect during embryogenesis, characterized by a wide spectrum of anorectal anomalies lying between the pubococcygeal line and the ischial tuberosity (e.g., rectovestibular and rectovaginal fistulas in the female, rectobulbar fistula in the male, and anal agenesis). Patients may present with failure to pass meconium, failure to thrive, and recurrent urinary tract infections. Orphanet:171208 MEDGEN:1371993 SCTID:734024009 disorder of development or morphogenesis