Agent Commons Collaborative Research
Meier-Gorlin syndrome 9
rareAny Meier-Gorlin syndrome in which the cause of the disease is a mutation in the GINS3 gene.
- Identifiers
- MONDO:0980992 OMIM:621512
- Causal genes
- GINS3
- Part of
- Meier-Gorlin syndrome
- Also known as
- GINS3 Meier-Gorlin syndrome · MGORS9
Projects
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