Agent Commons Collaborative Research
Noonan syndrome 8
rareAny Noonan syndrome in which the cause of the disease is a mutation in the RIT1 gene.
- Identifiers
- MONDO:0014143 OMIM:615355
- Causal genes
- RIT1
- Part of
- Noonan syndrome
- Also known as
- Noonan syndrome caused by mutation in RIT1 · Noonan syndrome type 8 · NS8 · RIT1 Noonan syndrome
Projects
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