syndromic intellectual disability pseudoaminopterin syndrome https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/6751 https://rarediseases.info.nih.gov/diseases/4544/pseudoaminopterin-syndrome https://www.malacards.org/card/aminopterin_syndrome_sine_aminopterin MONDO:0010865 icd11.foundation:893045173 Orphanet:221120 MESH:C535823 GARD:0004544 Pseudoaminopterin syndrome is a developmental anomalies syndrome that resembles the aminopterin embryopathy without history of fetal exposure to aminopterin. It is characterized by skull (craniosynostosis and poorly mineralized cranial vault), dysmorphic (ocular hypertelorism, palpebral fissure anomalies, micrognathia cleft lip and/or high arched palate and small and low set/rotated ears) and limb (brachydactyly, syndactyly and clinodactyly) anomalies, associated with mild-to-moderate intellectual deficit and short stature. aminopterin syndrome-like sine aminopterin aminopterin syndrome sine aminopterin UMLS:C0795939 pseudoaminopterin syndrome MEDGEN:163196 SCTID:715867000 OMIM:600325 ASSA multiple congenital anomalies/dysmorphic syndrome-intellectual disability syndromic craniosynostosis