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- Noonan_syndrome abstract "Noonan syndrome (NS) is a relatively common autosomal dominant congenital disorder that affects both males and females equally. It used to be referred to as the male version of Turner's syndrome (and is still sometimes described in this way); however, the genetic causes of Noonan syndrome and Turner syndrome are distinct. The principal features include congenital heart defect (typically pulmonary valve stenosis) also ASD, hypertrophic cardiomyopathy, short stature, learning problems, pectus excavatum, impaired blood clotting, and a characteristic configuration of facial features including a webbed neck and a flat nose bridge. The syndrome is named after Dr. Jacqueline Noonan. It is a RASopathy, as the syndrome is in the family of RAS-MAPK pathway disorders.It is believed that between approximately 1 in 1,000 and 1 in 2,500 children worldwide are born with NS. It is one of the most common genetic syndromes associated with congenital heart disease, similar in frequency to Down syndrome. However, the range and severity of features can vary greatly in patients with NS. Therefore, the syndrome is not always identified at an early age.".
- Noonan_syndrome diseasesdb "29094".
- Noonan_syndrome emedicineSubject "article".
- Noonan_syndrome emedicineTopic "947504".
- Noonan_syndrome icd10 "Q87.1".
- Noonan_syndrome icd9 "759.89".
- Noonan_syndrome medlineplus "001656".
- Noonan_syndrome meshId "D009634".
- Noonan_syndrome omim "163950".
- Noonan_syndrome thumbnail Noonan_syndrome.PNG?width=300.
- Noonan_syndrome wikiPageExternalLink noonan.
- Noonan_syndrome wikiPageExternalLink 001656.htm.
- Noonan_syndrome wikiPageExternalLink www.noonansyndrome.org.uk.
- Noonan_syndrome wikiPageExternalLink www.teamnoonan.org.
- Noonan_syndrome wikiPageExternalLink 2014-NSFC-Form.pdf.
- Noonan_syndrome wikiPageExternalLink 2014-NSFC-Packet-SMALL.pdf.
- Noonan_syndrome wikiPageExternalLink Brochure.pdf.
- Noonan_syndrome wikiPageExternalLink www.teamrasopathies.org.
- Noonan_syndrome wikiPageExternalLink Dyscerne_Noonan_Syndrome.pdf.
- Noonan_syndrome wikiPageExternalLink Noonansyndromefoundation.
- Noonan_syndrome wikiPageID "988477".
- Noonan_syndrome wikiPageRevisionID "603622108".
- Noonan_syndrome caption "A 12-year-old female with Noonan syndrome. Typical webbed neck. Double structural curve with rib deformity.".
- Noonan_syndrome diseasesdb "29094".
- Noonan_syndrome emedicinesubj "article".
- Noonan_syndrome emedicinetopic "947504".
- Noonan_syndrome hasPhotoCollection Noonan_syndrome.
- Noonan_syndrome icd "759.89".
- Noonan_syndrome icd "Q87.1".
- Noonan_syndrome medlineplus "1656".
- Noonan_syndrome meshid "D009634".
- Noonan_syndrome name "Noonan syndrome".
- Noonan_syndrome omim "163950".
- Noonan_syndrome wordnet_type synset-disease-noun-1.
- Noonan_syndrome subject Category:Autosomal_dominant_disorders.
- Noonan_syndrome subject Category:Congenital_heart_disease.
- Noonan_syndrome subject Category:Enzyme_defects.
- Noonan_syndrome subject Category:Genodermatoses.
- Noonan_syndrome subject Category:Intellectual_disability.
- Noonan_syndrome subject Category:RASopathies.
- Noonan_syndrome subject Category:Syndromes.
- Noonan_syndrome type Abstraction100002137.
- Noonan_syndrome type Attribute100024264.
- Noonan_syndrome type AutosomalDominantDisease114162025.
- Noonan_syndrome type AutosomalDominantDisorders.
- Noonan_syndrome type Cognition100023271.
- Noonan_syndrome type Complex105870365.
- Noonan_syndrome type Concept105835747.
- Noonan_syndrome type Condition113920835.
- Noonan_syndrome type Content105809192.
- Noonan_syndrome type Defect114464005.
- Noonan_syndrome type Disease114070360.
- Noonan_syndrome type EnzymeDefects.
- Noonan_syndrome type GeneticDisease114151139.
- Noonan_syndrome type Idea105833840.
- Noonan_syndrome type IllHealth114052046.
- Noonan_syndrome type Illness114061805.
- Noonan_syndrome type Imperfection114462666.
- Noonan_syndrome type PathologicalState114051917.
- Noonan_syndrome type PhysicalCondition114034177.
- Noonan_syndrome type PsychologicalFeature100023100.
- Noonan_syndrome type State100024720.
- Noonan_syndrome type Syndrome105870790.
- Noonan_syndrome type Syndromes.
- Noonan_syndrome type Whole105869584.
- Noonan_syndrome type Disease.
- Noonan_syndrome type Situation.
- Noonan_syndrome comment "Noonan syndrome (NS) is a relatively common autosomal dominant congenital disorder that affects both males and females equally. It used to be referred to as the male version of Turner's syndrome (and is still sometimes described in this way); however, the genetic causes of Noonan syndrome and Turner syndrome are distinct.".
- Noonan_syndrome label "Noonan syndrome".
- Noonan_syndrome label "Noonan-Syndrom".
- Noonan_syndrome label "Sindrome di Noonan".
- Noonan_syndrome label "Syndrome de Noonan".
- Noonan_syndrome label "Syndroom van Noonan".
- Noonan_syndrome label "Síndrome de Noonan".
- Noonan_syndrome label "Síndrome de Noonan".
- Noonan_syndrome label "Zespół Noonan".
- Noonan_syndrome label "Синдром Нунан".
- Noonan_syndrome label "متلازمة نونان".
- Noonan_syndrome sameAs Noonan-Syndrom.
- Noonan_syndrome sameAs Síndrome_de_Noonan.
- Noonan_syndrome sameAs Syndrome_de_Noonan.
- Noonan_syndrome sameAs Sindrome_di_Noonan.
- Noonan_syndrome sameAs 누난_증후군.
- Noonan_syndrome sameAs Syndroom_van_Noonan.
- Noonan_syndrome sameAs Zespół_Noonan.
- Noonan_syndrome sameAs Síndrome_de_Noonan.
- Noonan_syndrome sameAs m.03x0b8.
- Noonan_syndrome sameAs Q1543446.
- Noonan_syndrome sameAs Q1543446.
- Noonan_syndrome sameAs 846.
- Noonan_syndrome sameAs Noonan_syndrome.
- Noonan_syndrome wasDerivedFrom Noonan_syndrome?oldid=603622108.
- Noonan_syndrome depiction Noonan_syndrome.PNG.
- Noonan_syndrome isPrimaryTopicOf Noonan_syndrome.
- Noonan_syndrome name "Noonan syndrome".
