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...

16p12.1p12.3 triplication syndrome is a rare genetic disorder caused by the presence of three copies of a small segment of chromosome 16. It is characterized by developmental delays, intellectual disability, and a variety of physical features. Com...

16p13.11 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the short arm of chromosome 16. It is characterized by intellectual disability, developmental delays, and a variety of physical features. Other ...

16p13.11 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 intellectual d...

16p13.2 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the short arm of chromosome 16. It is characterized by intellectual disability, developmental delays, and physical abnormalities. Common features...

16p13.3 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 intellectual di...

16q24.1 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, including in...

16q24.3 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, including in...

17p11.2 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the short arm of chromosome 17. It is characterized by a variety of physical and developmental features, including intellectual disab...

17p13.3 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the short arm of chromosome 17. It is characterized by a wide range of physical and developmental features, including intellectual di...

17q11.2 microduplication syndrome is a rare genetic disorder caused by an extra copy of genetic material on the long arm of chromosome 17. It is characterized by a wide range of physical and developmental features, including intellectual disabilit...

17q12 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material on the long arm of chromosome 17. It is characterized by a wide range of physical and developmental features, including intellectua...

17q12 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the long arm of chromosome 17. It is characterized by a wide range of physical and developmental features, including intellectual disab...

17q21.31 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the long arm of chromosome 17. It is characterized by a wide range of physical and developmental features, including intellectual di...

17q23.1q23.2 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material from a specific region of chromosome 17. It is characterized by intellectual disability, developmental delays, and physical ...

17q24.2 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material from a specific region of chromosome 17. It is characterized by a wide range of physical and developmental features, including in...