Neu-Laxova syndrome https://github.com/monarch-initiative/mondo/issues/6749 https://github.com/monarch-initiative/mondo/issues/6878 https://github.com/monarch-initiative/mondo/issues/8566 https://www.malacards.org/card/neu_laxova_syndrome_1 MONDO:0000179 UMLS:C0265218 GARD:0000102 NLS MEDGEN:78537 MESH:C536405 SCTID:77817004 Neu Laxova syndrome Orphanet:2671 icd11.foundation:893358230 ICD9:759.89 OMIMPS:256520 Neu-Laxova syndrome (NLS) is a rare, multiple malformation syndrome characterized by severe intrauterine growth retardation (IUGR), severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. integumentary system disorder syndromic disease lissencephaly type 3 multiple congenital anomalies/dysmorphic syndrome-intellectual disability developmental anomaly of metabolic origin 3-phosphoglycerate dehydrogenase deficiency