Disease association ontology term - MONDO:0010463 - X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Term summary
- ID
- MONDO:0010463
- Name
- X-linked dominant chondrodysplasia, Chassaing-Lacombe type
- Ontology or CV name
- Disease association
- Definition
- A rare genetic bone disorder characterized by chondrodysplasia, intrauterine growth retardation (IUGR), hydrocephaly and facial dysmorphism in the affected males.
