Chondrodysplasia, generic
Phenotype Details
- Phene ID
- 374
- Name
- Chondrodysplasia, generic
- Phene Name
- N/A
- OMIA ID
- 187
- Species ID
- 9913
- Characterised
- No
- Characterised Year
- N/A
Summary
Information previously listed here relating the chondrodysplasia caused by mutations in the EVC2 (also called limbin) gene has been moved to 'OMIA:002540-9913 : Chondrodysplasia, EVC2-related in Bos taurus'. [22/03/2022].