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Diseases / Disorder of development or morphogenesis

Noonan syndrome and Noonan-related syndrome

rare

Identifiers: MONDO:0020297 Orphanet:98733
Part of: RASopathy Disorder of development or morphogenesis Familial hypertrophic cardiomyopathy

Subtypes

All diseases Rare only

Disease Rare Not rare Subtypes

Noonan syndrome MONDO:0018997 16
Cardiofaciocutaneous syndrome MONDO:0015280 4
Noonan syndrome with multiple lentigines MONDO:0007893 3
Noonan syndrome-like disorder with loose anagen hair MONDO:0011899 2
Costello syndrome MONDO:0009026 HRAS
Legius syndrome MONDO:0012669 SPRED1

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