ICD-10: M61.232

Hirata disease Donohue syndrome obsolete acroosteolysis Gamstorp-Wohlfart syndrome obsolete Saldino-Noonan syndrome obsolete Verma-Naumoff syndrome Ullrich congenital muscular dystrophy Fukuyama congenital muscular dystrophy cranioectodermal dysplasia glycogen storage disease XV acrocapitofemoral dysplasia Askin's tumor distal arthrogryposis atelosteogenesis Baller-Gerold syndrome Bart-Pumphrey syndrome Bethlem myopathy Birk-Barel syndrome Bjornstad syndrome Bowen-Conradi syndrome brachyolmia Brown-Vialetto-Van Laere syndrome AGAT deficiency Chanarin-Dorfman syndrome Qazi Markouizos syndrome ARC syndrome Meckel syndrome Ogden syndrome guanidinoacetate methyltransferase deficiency Kahrizi syndrome Kennedy's disease Cogan-Reese syndrome Adams-Oliver syndrome Baraitser-Winter syndrome Carpenter syndrome Warburg micro syndrome MASA syndrome Smith-McCort dysplasia omodysplasia CEDNIK syndrome Stormorken syndrome Galloway-Mowat syndrome 1 orofaciodigital syndrome IV stromal dystrophy EAST syndrome Schimke immuno-osseous dysplasia Barber-Say syndrome lethal congenital contracture syndrome 1 Holzgreve-Wagner-Rehder Syndrome 3MC syndrome 1 Yunis-Varon syndrome Nance-Horan syndrome ulnar-mammary syndrome lethal congenital contracture syndrome 3 lethal congenital contracture syndrome 4 Muenke Syndrome EEC syndrome Miles-Carpenter syndrome Christianson syndrome Pierson syndrome