syndromic intellectual disability Biemond syndrome type 2 https://github.com/monarch-initiative/mondo/issues/5588 https://rarediseases.info.nih.gov/diseases/882/biemond-syndrome-2 https://www.malacards.org/card/biemond_syndrome_ii Orphanet:141333 iris coloboma, intellectual disability, obesity, hypogenitalism, and postaxial polydactyly iris coloboma, mental retardation, obesity, hypogenitalism, and postaxial polydactyly UMLS:C1859487 SCTID:717887003 Biemond syndrome 2 Biemond syndrome type 2 (BS2) is a rare genetic neurological and developmental disorder reported in a very small number of patients with a poorly defined phenotype which includes iris coloboma, short stature, obesity, hypogonadism, postaxial polydactyly, and intellectual disability. Hydrocephalus and facial dysostosis were also reported. BS2 shares features with Bardet-Biedl syndrome. There have been no further descriptions in the literature since 1997. BS2 GARD:0000882 hypogonadism-short stature-coloboma-preaxial polydactyly syndrome Editor note: see also type 1, e.g. GARD:0000881 MONDO:0008864 MEDGEN:347159 Biemond syndrome type 2 OMIM:210350 MESH:C565902 multiple congenital anomalies/dysmorphic syndrome-intellectual disability