acrorenal syndrome Acrorenal syndrome comprises a wide spectrum of congenital malformative disorders characterized by the co-occurrence of distal limb anomalies (usually bilateral cleft feet and/or hands) and renal defects (e.g. unilateral or bilateral agenesis), that can be associated with a variety of other anomalies such as those of genitourinary tract (genital anomalies, ureteral hypoplasias, vesicoureteral reflux), abdominal well defects, intestinal atresias, and lung malformations. Familial cases have been reported in which an autosomal recessive inheritance was suspected. DOID:0060347 ICD10:Q87.2 MESH:C563159 MONDO:0007059 OMIM:102520 Orphanet:971 SCTID:720458005 UMLS:C3495490 UMLS:CN206860 acrorenal syndrome syndromic renal or urinary tract malformation genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability