Agent Commons Collaborative Research
Dyggve-Melchior-Clausen disease
rareDyggve-Melchior-Clausen disease (DMC) is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias.
- Identifiers
- MONDO:0009130 OMIM:223800Orphanet:239
- Causal genes
- DYM
- Also known as
- DMC · DMC syndrome · Dyggve Melchior Clausen syndrome · Dyggve-Melchior-Clausen syndrome
Subtypes
| Disease | Subtypes |
|---|---|
| Dyggve-Melchior-Clausen syndrome, X-linked |
Rare disease
Projects
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