Weissenbacher-Zweymueller syndrome; heterozygous otospondylomegaepiphyseal dysplasia

Genetics

• autosomal dominant
• associated with defects in COL11A2
• allelic with
  • Stickler syndrome type 3
  • autosomal recessive otospondylomegaepiphyseal dysplasia

More general terms

• genetic syndrome (multisystem disorder)

Database

• OMIM: https://mirror.omim.org/entry/277610