ICD-10: Q71.22

Charcot-Marie-Tooth disease type X muscular dystrophy-dystroglycanopathy type B1 ABCD syndrome Allan-Herndon-Dudley syndrome anauxetic dysplasia 1 obsolete anonychia congenita distal arthrogryposis atelosteogenesis Baller-Gerold syndrome Boomerang dysplasia brachyolmia obsolete Opitz-GBBB syndrome Ogden syndrome CHARGE syndrome Marshall-Smith syndrome IMAGe syndrome Townes-Brocks syndrome janus kinase-3 deficiency acrofrontofacionasal dysostosis Adams-Oliver syndrome Carpenter syndrome Van Maldergem syndrome Smith-McCort dysplasia omodysplasia Ohdo syndrome, SBBYS variant acrofacial dysostosis Cincinnati type Galloway-Mowat syndrome 1 Hennekam syndrome orofaciodigital syndrome IV orofaciodigital syndrome V acrofacial dysostosis acrofacial dysostosis Rodriguez type chondrodysplasia Blomstrand type chromosomal deletion syndrome chromosome 4q21 deletion syndrome chromosome 5q12 deletion syndrome chromosome 19p13.13 deletion syndrome fibrochondrogenesis MEDNIK syndrome Barber-Say syndrome lethal congenital contracture syndrome 2 Ritscher-Schinzel syndrome 2 Nance-Horan syndrome fetal encasement syndrome lethal congenital contracture syndrome 3 Muenke Syndrome Pierson syndrome Gamstorp-Wohlfart syndrome obsolete SC phocomelia syndrome