ICD-10: M61

mesocestoidiasis obsolete peripheral dysostosis mulibrey nanism Donohue syndrome Carney complex Gamstorp-Wohlfart syndrome Charcot-Marie-Tooth disease type 2 hypermethioninemia obsolete Verma-Naumoff syndrome Walker-Warburg syndrome muscular dystrophy-dystroglycanopathy type B1 glycogen storage disease IX Allan-Herndon-Dudley syndrome Bart-Pumphrey syndrome Bethlem myopathy Birk-Barel syndrome Bjornstad syndrome Bowen-Conradi syndrome Brody myopathy Dent disease COX deficiency, infantile mitochondrial myopathy tyrosinemia type II autosomal dominant disease Qazi Markouizos syndrome rapadilino syndrome Kahrizi syndrome obsolete Jensen syndrome Koolen de Vries syndrome IMAGe syndrome autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 1 Miles-Carpenter syndrome Christianson syndrome Griscelli syndrome type 1 Griscelli syndrome type 3 obsolete Muscle calcification and ossification Townes-Brocks syndrome amyotrophic lateral sclerosis type 18 MASA syndrome Smith-McCort dysplasia Ohdo syndrome Ohdo syndrome, SBBYS variant parameningeal embryonal rhabdomyosarcoma Native American myopathy acrorenal syndrome Galloway-Mowat syndrome 1 orofaciodigital syndrome III chondrodysplasia Blomstrand type Cole-Carpenter syndrome chromosome 2q31.1 duplication syndrome fibrochondrogenesis MEDNIK syndrome EAST syndrome Schimke immuno-osseous dysplasia Barber-Say syndrome lethal congenital contracture syndrome 2 Char syndrome Holzgreve-Wagner-Rehder Syndrome Ritscher-Schinzel syndrome 1 3MC syndrome 1 3MC syndrome 2 Yunis-Varon syndrome Nance-Horan syndrome Muenke Syndrome