ICD-10: M89.25

Hirata disease campomelic dysplasia Gamstorp-Wohlfart syndrome spondylocostal dysostosis brachydactyly Baller-Gerold syndrome Bethlem myopathy Boomerang dysplasia Brody myopathy PSAT deficiency Meckel syndrome proximal symphalangism Ehlers-Danlos syndrome spondylodysplastic type 2 Perrault syndrome Carpenter syndrome Smith-McCort dysplasia Simpson-Golabi-Behmel syndrome type 1 sclerosteosis omodysplasia Meier-Gorlin syndrome chondrodysplasia Blomstrand type chromosome 10q23 deletion syndrome Cole-Carpenter syndrome fibrochondrogenesis Schimke immuno-osseous dysplasia Warsaw breakage syndrome Holzgreve-Wagner-Rehder Syndrome autosomal dominant Robinow syndrome 3 Wilson-Turner syndrome Miles-Carpenter syndrome