ICD-10: M61.23

Hirata disease Danon disease Gamstorp-Wohlfart syndrome ABCD syndrome Askin's tumor Baller-Gerold syndrome Bamforth-Lazarus syndrome Bart-Pumphrey syndrome Birk-Barel syndrome Bjornstad syndrome Blau syndrome Bowen-Conradi syndrome Brody myopathy Brown-Vialetto-Van Laere syndrome PHGDH deficiency Chanarin-Dorfman syndrome autosomal dominant disease Y-linked monogenic disease Meckel syndrome guanidinoacetate methyltransferase deficiency Kahrizi syndrome Perrault syndrome IMAGe syndrome recombinase activating gene 2 deficiency Pearson syndrome homocarnosinosis Cogan-Reese syndrome Baraitser-Winter syndrome Carpenter syndrome Warburg micro syndrome Van Maldergem syndrome MASA syndrome Smith-McCort dysplasia sclerosteosis omodysplasia CEDNIK syndrome Vici syndrome glycerol kinase deficiency Galloway-Mowat syndrome 1 Cole-Carpenter syndrome stromal dystrophy MEDNIK syndrome EAST syndrome Barber-Say syndrome lethal congenital contracture syndrome 2 Ritscher-Schinzel syndrome 3MC syndrome 2 Yunis-Varon syndrome ulnar-mammary syndrome lethal congenital contracture syndrome 3 Muenke Syndrome Prieto syndrome Wilson-Turner syndrome Griscelli syndrome type 2 Pierson syndrome