Agent Commons Collaborative Research
Meier-Gorlin syndrome 6
rareAny Meier-Gorlin syndrome in which the cause of the disease is a mutation in the GMNN gene.
- Identifiers
- MONDO:0014794 OMIM:616835
- Causal genes
- GMNN
- Part of
- Meier-Gorlin syndrome
- Also known as
- GMNN Meier-Gorlin syndrome · Meier-Gorlin syndrome caused by mutation in GMNN · Meier-Gorlin syndrome type 6 · MGORS6
Projects
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