OBO ID: DOID:0060580 |
Term Name: | Noonan syndrome 2 | Search Ontology: | |
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Definition: | A Noonan syndrome characterized by hypertrophic obstructive cardiomyopathy and that has_material_basis_in an autosomal recessive inheritance. https://www.ncbi.nlm.nih.gov/pubmed/5782826 | ||
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Ontology: | Human Disease ( DOID:0060580 ) |
OTHER Noonan syndrome 2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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