eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | c syndrome |
| Comorbidity | C0028326|noonan syndrome |
| Sentences | 2 |
| PubMedID- 24068150 | noonan syndrome is one of the most common genetic syndromes and also an important differential diagnosis in children presenting with syndromic facies similar to turner's syndrome phenotype. |
| PubMedID- 23373411 | noonan syndrome (ns) is one of the most frequent dysmorphic syndromes in children with a frequency of 1/1000-1/2500 of newborns. |
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