syndromic intellectual disability congenital nervous system disorder Ulbright-Hodes syndrome GARD:0005394 ICD10:Q87.8 MESH:C537754 MONDO:0009963 OMIM:266910 Orphanet:3404 RL syndrome SCTID:719840003 UMLS:C1849438 Ulbright Hodes syndrome Ulbright-Hodes syndrome is characterised by renal dysplasia, growth retardation, phocomelia or mesomelia, radiohumeral fusion, rib abnormalities, anomalies of the external genitalia and a potter-like facies. The syndrome has been described in three infants (one pair of sibs and an unrelated case), all of whom died shortly after birth from respiratory distress resulting from pulmonary hypoplasia and oligohydramnios caused by renal dysplasia. The mode of transmission appears to be autosomal recessive. renal dysplasia limb defects syndrome renal dysplasia, mesomelia, and radiohumeral fusion renal dysplasia-limb defects syndrome renal dysplasia-mesomelia-radiohumeral fusion syndrome multiple congenital anomalies/dysmorphic syndrome-intellectual disability syndromic urogenital tract malformation syndromic renal or urinary tract malformation