OBO ID: DOID:0112170 |
Term Name: | Noonan syndrome 12 | Search Ontology: | |
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Definition: | A Noonan syndrome characterized by macrocephaly, facial anomalies including hypertelorism, downslanting palpebral fissures, and low-set ears, and other Noonan syndrome features that has_material_basis_in heterozygous mutation in the RRAS2 gene on chromosome 11p15.2. (2) | ||
References: | |||
Ontology: | Human Disease ( DOID:0112170 ) |
OTHER Noonan syndrome 12 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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