ICD-10: Q60.4

Hirata disease monogenic disease campomelic dysplasia Donohue syndrome Alstrom syndrome obsolete Majewski syndrome ABCD syndrome Bjornstad syndrome Boomerang dysplasia brachyolmia autosomal genetic disease adenylosuccinase lyase deficiency guanidinoacetate methyltransferase deficiency Marshall-Smith syndrome Koolen de Vries syndrome Pearson syndrome renal-hepatic-pancreatic dysplasia Rapp-Hodgkin syndrome acrorenal syndrome chondrodysplasia Blomstrand type chromosome 4q21 deletion syndrome chromosome 17q21.31 duplication syndrome MEDNIK syndrome Holzgreve-Wagner-Rehder Syndrome Yunis-Varon syndrome chondrodysplasia-pseudohermaphroditism syndrome Muenke Syndrome Wilson-Turner syndrome Griscelli syndrome type 3 Pierson syndrome septooptic dysplasia renal hypoplasia renal coloboma syndrome oligomeganephronia