autosomal recessive disease Fraser syndrome DOID:0090001 Fraser syndrome Fraser syndrome is a rare clinical entity including as main characteristics cryptophthalmos and syndactyly. Fraser-Francois syndrome GARD:0006465 ICD10:Q87.0 MESH:D058497 MONDO:0009046 Meyer-Schwickerath's syndrome NCIT:C118436 OMIMPS:219000 Orphanet:2052 SCTID:204102004 UMLS:C0265233 Ulrich-Feichtiger syndrome cryptophthalmos syndrome cryptophthalmos with Other malformations cryptophthalmos with other malformations cryptophthalmos-syndactyly syndrome cyclopism https://rarediseases.info.nih.gov/diseases/6465/fraser-syndrome syndromic developmental defect of the eye syndromic anorectal malformation syndromic urogenital tract malformation syndromic genetic deafness syndromic renal or urinary tract malformation cryptophthalmia genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability