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Noonan syndrome and Noonan-related syndrome | RareConnect | RareConnect.io

/disorder of development or morphogenesis

/familial hypertrophic cardiomyopathy

/Noonan syndrome and Noonan-related syndrome

Noonan syndrome and Noonan-related syndrome

Rare Disease

MONDO:0020297

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Orphanet

Orphanet:98733 ↗

GARD

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