Jackson-Weiss syndrome
https://rarediseases.info.nih.gov/diseases/6796/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
MONDO:0007400
UMLS:C0795998
JWS
MESH:C537559
GARD:6796
acrocephalosyndactyly