syndromic intellectual disability hepatic fibrosis-renal cysts-intellectual disability syndrome GARD:0005177 Hepatic fibrosis-renal cysts-intellectual disability syndrome is a rare, syndromic intellectual disability characterized by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnea. There have been no further descriptions in the literature since 1987. MESH:C565867 MONDO:0008941 OMIM:213010 Orphanet:2031 Thompson Baraitser syndrome Thompson-Baraitser syndrome cerebellar vermis aplasia with associated features suggesting SMITH-Lemli-Opitz syndrome and Meckel syndrome genetic parenchymatous liver disease genetic nervous system disorder familial cystic renal disease