11p15.4 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the short arm of chromosome 11. It is characterized by a variety of physical and developmental features, including intellectual disab...

11q22.2q22.3 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the long arm of chromosome 11. It is characterized by intellectual disability, developmental delay, and a variety of physical features. Othe...

12q14 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the long arm of chromosome 12. It is characterized by a wide range of physical and developmental features, including intellectual disability, delay...

12q15q21.1 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material from a specific region of chromosome 12. It is characterized by intellectual disability, developmental delay, and a variety of physical features....

13q12.3 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the long arm of chromosome 13. It is characterized by a wide range of physical and developmental features, including intellectual disability, del...

14q11.2 microdeletion syndrome is a rare genetic disorder caused by a missing piece of genetic material on the long arm of chromosome 14. It is characterized by a wide range of physical and developmental features, including intellectual disability...

14q11.2 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the long arm of chromosome 14. It is characterized by a wide range of physical and developmental features, including intellectual dis...

14q22q23 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the long arm of chromosome 14. It is characterized by a wide range of physical and developmental abnormalities, including intellectual disabilit...

14q24.1q24.3 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material from a specific region of chromosome 14. It is characterized by intellectual disability, developmental delay, and a variety of physical feature...

14q32 duplication syndrome is a rare genetic disorder caused by a duplication of genetic material on the long arm of chromosome 14. It is characterized by a wide range of physical and developmental abnormalities, including intellectual disability,...

15q Overgrowth Syndrome is a rare genetic disorder caused by a duplication of the long arm of chromosome 15. It is characterized by physical overgrowth, developmental delays, and a variety of other medical issues. Common features include macroceph...

15q11.2 microdeletion syndrome is a rare genetic disorder caused by a missing piece of genetic material on the long arm of chromosome 15. It is characterized by intellectual disability, developmental delays, speech and language delays, and behavio...

15q11q13 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the long arm of chromosome 15. It is characterized by a wide range of physical and developmental features, including intellectual di...

15q13.3 microdeletion syndrome is a rare genetic disorder caused by a small deletion of genetic material on the long arm of chromosome 15. It is associated with a wide range of physical and cognitive disabilities, including intellectual disability...

15q14 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the long arm of chromosome 15. It is characterized by intellectual disability, developmental delays, and physical abnormalities. Symptoms can vary ...

16p11.2p12.2 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material from a specific region of chromosome 16. It is characterized by a wide range of physical and developmental features, includi...

16p11.2p12.2 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the short arm of chromosome 16. It is characterized by a wide range of physical and developmental features, including intellectu...