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Weissenbacher-Zweymueller syndrome; heterozygous otospondylomegaepiphyseal dysplasia
Genetics:
- autosomal dominant
- associated with defects in COL11A2
- allelic with
- Stickler syndrome type 3
- autosomal recessive otospondylomegaepiphyseal dysplasia
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 277610
References
OMIM :accession 277610