has material basis in autosomal recessive disease acrorenal syndrome SNOMEDCT_US_2025_09_01:720458005 MIM:201310 disease_ontology UMLS_CUI:C3495490 MESH:C563159 MIM:102520 2015-06-04T14:51:42Z A syndrome characterized by limb defects, usually bilateral, like cleft hands or feet and longitudinal defects involving radius or ulna, tibia or fibula and renal anomalies which include agenesis, hypoplasia and rarely polycystic kidneys. Additional malformations may involve the oro-mandibular region, the trachea and lungs, skin derivatives including sweat glands, mammary glands, the uterus, vas deferens, the nasal placodes and the eyes. DOID:0060347 syndrome autosomal recessive inheritance