OBO ID: DOID:0112169 |
Term Name: | Noonan syndrome 11 | Search Ontology: | |
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Definition: | A Noonan syndrome characterized by clinical characteristics of Noonan syndrome, varying impairment of intellectual development, and cardiac hypertrophy that has_material_basis_in heterozygous mutation in the MRAS gene on chromosome 3q22.3. https://pubmed.ncbi.nlm.nih.gov/28289718/ | ||
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Ontology: | Human Disease ( DOID:0112169 ) |
OTHER Noonan syndrome 11 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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