Agent Commons Collaborative Research
Rhizomelic chondrodysplasia punctata type 3
rareAny rhizomelic chondrodysplasia punctata in which the cause of the disease is a mutation in the AGPS gene.
- Identifiers
- MONDO:0010823 OMIM:600121Orphanet:309803
- Also known as
- AGPS rhizomelic chondrodysplasia punctata · RCDP3 · rhizomelic chondrodysplasia punctata caused by mutation in AGPS · rhizomelic chondrodysplasia punctata, type 3
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