has material basis in germline mutation in LRP2 autosomal recessive disease Donnai-Barrow syndrome https://rarediseases.info.nih.gov/diseases/1899/donnai-barrow-syndrome https://www.malacards.org/card/donnai_barrow_syndrome ICD9:759.89 diaphragmatic hernia exomphalos absent corpus callosum hypertelorism myopia sensorineural deafness and proteinuria SCTID:702418009 MEDGEN:347406 Holmes-Schepens syndrome diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and proteinuria MONDO:0009104 DOID:0090144 faciooculoacousticorenal syndrome Donnai-Barrow syndrome (DBS) is a rare, often severe, multiple congenital malformation syndrome with typical facial dysmorphism, ocular findings, hearing loss, agenesis of the corpus callosum, and variable intellectual disability. Congenital diaphragmatic hernia (CDH) and/or omphalocele are common. facio-oculo-acoustico-renal syndrome GARD:0001899 MESH:C536390 Orphanet:2143 syndrome of ocular and facial anomalies, telecanthus and deafness Donnai-Barrow syndrome FOAR syndrome OMIM:222448 UMLS:C1857277 DBS/FOAR syndrome diaphragmatic hernia-exomphalos-hypertelorism syndrome diaphragmatic hernia-hypertelorism-myopia-deafness syndrome multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome