syndromic intellectual disability
Ulbright-Hodes syndrome
https://github.com/monarch-initiative/mondo/issues/5588
renal dysplasia, mesomelia, and radiohumeral fusion
OMIM:266910
Ulbright-Hodes syndrome is characterized 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.
GARD:5394
Orphanet:3404
renal dysplasia limb defects syndrome
SCTID:719840003
Ulbright Hodes syndrome
renal dysplasia-limb defects syndrome
MONDO:0009963
RL syndrome
renal dysplasia-mesomelia-radiohumeral fusion syndrome
MESH:C537754
UMLS:C1849438
multiple congenital anomalies/dysmorphic syndrome-intellectual disability