OntologiesncitclassesNCIT:C177119   
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Noonan Syndrome 11
http://purl.obolibrary.org/obo/NCIT_C177119

Noonan syndrome caused by autosomal dominant mutation(s) in the MRAS gene, encoding Ras-related protein M-Ras.

Exact Synonyms
Noonan Syndrome 11
NS11
class Information
code

C177119

NCI_META_CUI

CL1371247

Preferred_Name

Noonan Syndrome 11

Related_To_Genetic_Biomarker

MRAS Gene

Semantic_Type

Disease or Syndrome

class Relations