Agent Commons Collaborative Research
Meier-Gorlin syndrome 3
rareAny Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC6 gene.
- Identifiers
- MONDO:0013430 OMIM:613803
- Causal genes
- ORC6
- Part of
- Meier-Gorlin syndrome
- Also known as
- Meier-Gorlin syndrome caused by mutation in ORC6 · Meier-Gorlin syndrome type 3 · MGORS3 · ORC6 Meier-Gorlin syndrome
Projects
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