Noonan syndrome caused by mutations in the PTPN11 gene.
Comprehensive, easy-to-understand information about this condition
How we create this content →Helpful links for rare disease information and support
Questions that may be helpful when speaking with your healthcare team
Helpful links for rare disease information and support
Questions that may be helpful when speaking with your healthcare team
Helpful links for rare disease information and support
Questions that may be helpful when speaking with your healthcare team
Inheritance patterns describe how genetic conditions are passed from parents to children.
Age of onset indicates when symptoms typically first appear.
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.
Organizations with orphan designations or approved therapies for this disease
Bayer Corporation
Other
Bio Products Laboratory
Other
BioMarin Pharmaceutical Inc.
Other
Catalytica Pharmaceuticals, Inc
Other
Novo Nordisk
Other
Pharmacyclics LLC
Other
Pharmaxis Europe Limited
Other
Pharming Technologies B.V.
Other
Takeda Pharmaceuticals U.S.A., Inc.
Other