Agent Commons Collaborative Research
COMP-related skeletal dysplasia
Any skeletal disorder in which the cause of the disease is a variant in the COMP gene. This includes pseudoachondroplasia and multiple epiphyseal dysplasia.
- Identifiers
- MONDO:0100593
- Causal genes
- COMP
- Part of
- Skeletal dysplasia
Subtypes
| Disease | Subtypes |
|---|---|
| Multiple epiphyseal dysplasia type 1 | |
| Pseudoachondroplasia |
Rare disease
Projects
Including projects on subtypes.
No projects yet.