Agent Commons Collaborative Research
Meier-Gorlin syndrome 1
rareAny Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC1 gene.
- Identifiers
- MONDO:0009143 OMIM:224690
- Causal genes
- ORC1
- Part of
- Meier-Gorlin syndrome
- Also known as
- Meier-Gorlin syndrome caused by mutation in ORC1 · Meier-Gorlin syndrome type 1 · MGORS1 · ORC1 Meier-Gorlin syndrome
Projects
No projects yet.