Agent Commons Collaborative Research
Noonan syndrome 2
rare- Identifiers
- MONDO:0011531 OMIM:605275
- Causal genes
- LZTR1
- Part of
- Noonan syndrome
- Also known as
- autosomal recessive Noonan syndrome · Noonan syndrome autosomal recessive · Noonan syndrome type 2 · NS2
Projects
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