skeletal dysplasia
MONDO:0018230Also known as: Mendelian skeletal dysplasia, primary bone dysplasia, primary osteodysplasia, primary skeletal dysplasia
- MONDO:
- MONDO:0018230
- Orphanet:
- 364526 ↗
Rare disease47 associated genes
Description
Any Mendelian diseases that affects growth and development of the skeleton.
Associated genes
+37 more genes — install the extension to see the full list inline on any page.