Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Noonan_syndrome> ?p ?o }
- Noonan_syndrome wikiPageWikiLink Micrognathia.
- Noonan_syndrome wikiPageWikiLink Micrognathism.
- Noonan_syndrome wikiPageWikiLink Mitogen-activated_protein_kinase.
- Noonan_syndrome wikiPageWikiLink Motor_development.
- Noonan_syndrome wikiPageWikiLink Motor_neuron.
- Noonan_syndrome wikiPageWikiLink Muscle_pain.
- Noonan_syndrome wikiPageWikiLink Mutation.
- Noonan_syndrome wikiPageWikiLink Myalgia.
- Noonan_syndrome wikiPageWikiLink NRAS_(gene).
- Noonan_syndrome wikiPageWikiLink Neuroblastoma_RAS_viral_oncogene_homolog.
- Noonan_syndrome wikiPageWikiLink Neurofibromatosis-Noonan_syndrome.
- Noonan_syndrome wikiPageWikiLink Neurofibromin_2.
- Noonan_syndrome wikiPageWikiLink Nevus.
- Noonan_syndrome wikiPageWikiLink Noonan_Syndrome_with_Multiple_Lentigines.
- Noonan_syndrome wikiPageWikiLink Nystagmus.
- Noonan_syndrome wikiPageWikiLink OMIM.
- Noonan_syndrome wikiPageWikiLink Online_Mendelian_Inheritance_in_Man.
- Noonan_syndrome wikiPageWikiLink Otitis_media.
- Noonan_syndrome wikiPageWikiLink PTPN11.
- Noonan_syndrome wikiPageWikiLink Partial_thromboplastin_time.
- Noonan_syndrome wikiPageWikiLink Pathologic_nystagmus.
- Noonan_syndrome wikiPageWikiLink Pectus_carinatum.
- Noonan_syndrome wikiPageWikiLink Pectus_excavatum.
- Noonan_syndrome wikiPageWikiLink Pediatrics.
- Noonan_syndrome wikiPageWikiLink Pervasive_developmental_disorder.
- Noonan_syndrome wikiPageWikiLink Proptosis.
- Noonan_syndrome wikiPageWikiLink Protein_tyrosine_phosphatase.
- Noonan_syndrome wikiPageWikiLink Ptosis_(eyelid).
- Noonan_syndrome wikiPageWikiLink Pulmonary_stenosis.
- Noonan_syndrome wikiPageWikiLink Pulmonary_valve_stenosis.
- Noonan_syndrome wikiPageWikiLink Pulmonic_stenosis.
- Noonan_syndrome wikiPageWikiLink RAF1.
- Noonan_syndrome wikiPageWikiLink RASopathy.
- Noonan_syndrome wikiPageWikiLink Ras_subfamily.
- Noonan_syndrome wikiPageWikiLink Receptor_(biochemistry).
- Noonan_syndrome wikiPageWikiLink SHOC2.
- Noonan_syndrome wikiPageWikiLink SOS1.
- Noonan_syndrome wikiPageWikiLink Scapula.
- Noonan_syndrome wikiPageWikiLink Scoliosis.
- Noonan_syndrome wikiPageWikiLink Section_504_of_the_Rehabilitation_Act.
- Noonan_syndrome wikiPageWikiLink Short_stature.
- Noonan_syndrome wikiPageWikiLink Signal_transduction.
- Noonan_syndrome wikiPageWikiLink Speech-language_pathology.
- Noonan_syndrome wikiPageWikiLink Strabismus.
- Noonan_syndrome wikiPageWikiLink Swallowing_difficulties.
- Noonan_syndrome wikiPageWikiLink Thrombocytopenia.
- Noonan_syndrome wikiPageWikiLink Turner_syndrome.
- Noonan_syndrome wikiPageWikiLink Turners_syndrome.
- Noonan_syndrome wikiPageWikiLink University_of_Iowa.
- Noonan_syndrome wikiPageWikiLink Ventricular_septal_defect.
- Noonan_syndrome wikiPageWikiLink Vomiting.
- Noonan_syndrome wikiPageWikiLink Von_Willebrand_disease.
- Noonan_syndrome wikiPageWikiLink Watson_syndrome.
- Noonan_syndrome wikiPageWikiLink Webbed_neck.
- Noonan_syndrome wikiPageWikiLink Wide_spaced_eyes.
- Noonan_syndrome wikiPageWikiLink File:Autosomal_dominant_-_en.svg.
- Noonan_syndrome wikiPageWikiLink File:Noonan1883.JPG.
- Noonan_syndrome wikiPageWikiLinkText "Noonan syndrome".
- Noonan_syndrome wikiPageWikiLinkText "noonan syndrome".
- Noonan_syndrome caption "A 12-year-old girl 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 field Medical_genetics.
- Noonan_syndrome field Pediatrics.
- Noonan_syndrome genereviewsname "Noonan Syndrome".
- Noonan_syndrome genereviewsnbk "NBK1124".
- 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 wikiPageUsesTemplate Template:Authority_control.
- Noonan_syndrome wikiPageUsesTemplate Template:Commons_category.
- Noonan_syndrome wikiPageUsesTemplate Template:Deficiencies_of_intracellular_signaling_peptides_and_proteins.
- Noonan_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Noonan_syndrome wikiPageUsesTemplate Template:OMIM2.
- Noonan_syndrome wikiPageUsesTemplate Template:Phakomatoses_and_other_congenital_malformations_not_elsewhere_classified.
- Noonan_syndrome wikiPageUsesTemplate Template:Reflist.
- Noonan_syndrome wikiPageUsesTemplate Template:Rp.
- Noonan_syndrome wikiPageUsesTemplate Template:See_also.
- Noonan_syndrome wikiPageUsesTemplate Template:TOC_limit.
- 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 Article.
- Noonan_syndrome type Disease.
- Noonan_syndrome type Article.
- Noonan_syndrome type Defect.
- Noonan_syndrome type Disorder.
- Noonan_syndrome type Syndrome.
- Noonan_syndrome type Thing.
- Noonan_syndrome type Q12136.
- Noonan_syndrome comment "Noonan syndrome (NS) is a relatively common autosomal dominant congenital disorder that affects both males and females. It is 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.".