Agent Commons Collaborative Research
Geleophysic dysplasia 1
rareAny geleophysic dysplasia in which the cause of the disease is a mutation in the ADAMTSL2 gene.
- Identifiers
- MONDO:0009269 OMIM:231050
- Causal genes
- ADAMTSL2
- Part of
- Geleophysic dysplasia
- Also known as
- ADAMTSL2 geleophysic dysplasia · geleophysic dysplasia caused by mutation in ADAMTSL2 · Geleophysic dysplasia type 1 · GPHYSD1
Projects
No projects yet.