syndromic intellectual disability syndromic disease Wiedemann-Rautenstrauch syndrome https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/6744 https://github.com/monarch-initiative/mondo/issues/8101 https://www.malacards.org/card/wiedemann_rautenstrauch_syndrome Wiedemann Rautenstrauch syndrome MEDGEN:140806 Wiedemann Rautenstrauch Syndrome MESH:C536423 Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism. Wiedemann-Rautenstrauch syndrome SCTID:238874008 GARD:0000330 progeroid syndrome neonatal UMLS:C0406586 OMIM:264090 ICD9:259.8 Orphanet:3455 NCIT:C121565 progeroid syndrome, neonatal neonatal progeroid syndrome MONDO:0009910 NORD:1852 DOID:0081333 multiple congenital anomalies/dysmorphic syndrome-intellectual disability developmental anomaly of metabolic origin progeroid syndrome hereditary lipodystrophy POLR3A-related disorder osteogenesis imperfecta and a reduction of bone mineral density.