7q11.23 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the long arm of chromosome 7. It is characterized by a wide range of physical and developmental features, including intellectual disa...

7q31 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the long arm (q) of chromosome 7. It is characterized by a variety of physical and developmental abnormalities, including intellectual disability, d...

8p inverted duplication/deletion syndrome is a rare genetic disorder caused by a chromosomal abnormality. It is caused by a rearrangement of genetic material on the short arm of chromosome 8, resulting in an inverted duplication or deletion of gen...

8p11.2 deletion syndrome is a rare genetic disorder caused by a deletion of genetic material from a specific region of chromosome 8. It is characterized by a variety of physical and developmental abnormalities, including intellectual disability, d...

8p23.1 duplication syndrome is a rare genetic disorder caused by a duplication of a small section of chromosome 8. It is characterized by a variety of physical and developmental abnormalities, including intellectual disability, delayed development...

8p23.1 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the short arm of chromosome 8. It is characterized by a wide range of physical and developmental features, including intellectual disability, dela...

8q12 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the long arm of chromosome 8. It is characterized by a wide range of physical and developmental features, including intellectual disabil...

8q21.11 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material from a specific location on chromosome 8. It is characterized by intellectual disability, developmental delay, and a variety of p...

8q22.1 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material from a specific location on the long arm of chromosome 8. It is characterized by a variety of physical and developmental abnormali...

8q24.3 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material from a specific region of chromosome 8. It is characterized by a wide range of physical and developmental abnormalities, including...

9p13 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the short arm of chromosome 9. It is characterized by intellectual disability, developmental delays, and physical abnormalities. Common features inc...

9q21.13 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material from a specific region of chromosome 9. It is characterized by intellectual disability, developmental delay, and a variety of phy...

9q31.1q31.3 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material from the long arm of chromosome 9. It is characterized by intellectual disability, developmental delay, and a variety of phys...

9q33.3q34.11 microdeletion syndrome is a rare genetic disorder caused by the deletion of a small piece of genetic material from the long arm of chromosome 9. It is characterized by intellectual disability, developmental delay, and a variety of phy...

AA amyloidosis is a rare type of amyloidosis caused by the buildup of abnormal proteins called amyloid A (AA) in the body's organs and tissues. It is a systemic disorder, meaning it can affect multiple organs and systems in the body. AA amyloidosi...

AApoAIV amyloidosis is a rare, inherited form of amyloidosis caused by a mutation in the apolipoprotein A-IV gene. It is characterized by the buildup of amyloid deposits in the heart, kidneys, and other organs, leading to organ dysfunction and fai...

Aarskog Syndrome, also known as Aarskog-Scott Syndrome, is a rare genetic disorder that affects physical and mental development. It is caused by a mutation in the X-chromosome and is characterized by short stature, facial abnormalities, skeletal m...