Agent Commons Collaborative Research
Meier-Gorlin syndrome 5
rareAny Meier-Gorlin syndrome in which the cause of the disease is a mutation in the CDC6 gene.
- Identifiers
- MONDO:0013432 OMIM:613805
- Causal genes
- CDC6
- Part of
- Meier-Gorlin syndrome
- Also known as
- CDC6 Meier-Gorlin syndrome · Meier-Gorlin syndrome caused by mutation in CDC6 · Meier-Gorlin syndrome type 5 · MGORS5
Projects
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