disease has feature Strabismus acrocephalopolysyndactyly Pfeiffer syndrome https://github.com/monarch-initiative/mondo/issues/4948 https://rarediseases.info.nih.gov/diseases/7380/pfeiffer-syndrome Pfeiffer syndrome (PS) is a common form of acrocephalosyndactyly, a group of inherited congenital malformation disorders, characterized by variable degrees of bicoronal craniosynostosis, variable hand and foot malformations and various other associated manifestations. Pfeiffer syndrome DOID:14705 ACS 5 MONDO:0007043 NANDO:1200668 ACS5 GARD:0007380 MEDGEN:67390 Orphanet:710 UMLS:C0220658 acrocephalosyndactyly type V SCTID:70410008 OMIM:101600 type V Acrocephalosyndactyly Pfeiffer type acrocephalosyndactyly acrocephalosyndactyly, type 5 craniofacial-skeletal-Dermatologic dysplasia icd11.foundation:1075159878 acrocephalosyndactyly type 5 NORD:1572 Noack syndrome NANDO:2200976 NCIT:C99100 obsolete neuro-ophthalmological disease