acrorenal syndrome https://www.malacards.org/card/acrorenal_syndrome MESH:C563159 icd11.foundation:1948375645 GARD:0000514 OMIM:102520 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. MEDGEN:501193 SCTID:720458005 MONDO:0007059 Orphanet:971 UMLS:C3495490 DOID:0060347 acrorenal syndrome multiple congenital anomalies/dysmorphic syndrome without intellectual disability