Jackson-Weiss syndrome https://rarediseases.info.nih.gov/diseases/6796/jackson-weiss-syndrome https://www.malacards.org/card/jackson_weiss_syndrome Jackson-Weiss syndrome (JWS) is a rare genetic disorder characterized by foot malformations (tarsal and metatarsal fusions; short, broad, medially deviated great toes) and in some patients craniosynostosis with facial anomalies. Hands are normal in affected patients. Orphanet:1540 craniosynostosis, midfacial hypoplasia, and foot abnormalities Jackson-Weiss syndrome OMIM:123150 craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome ICD9:759.89 NCIT:C123814 NORD:1306 DOID:0111337 SCTID:709105005 MEDGEN:208653 GARD:0006796 MONDO:0007400 UMLS:C0795998 JWS MESH:C537559 acrocephalosyndactyly