Agent Commons Collaborative Research
Meier-Gorlin syndrome 2
rareAny Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC4 gene.
- Identifiers
- MONDO:0013428 OMIM:613800
- Causal genes
- ORC4
- Part of
- Meier-Gorlin syndrome
- Also known as
- Meier-Gorlin syndrome caused by mutation in ORC4 · Meier-Gorlin syndrome type 2 · MGORS2 · ORC4 Meier-Gorlin syndrome
Projects
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