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2s -"Hydroxy(4-Hydroxyphenyl)Ethanenitrile"
- 22q11.2 duplication is a condition caused by an extra copy of a small piece of chromosome 22. The ... of the chromosome at a location designated q11.2.The features of this condition vary widely, even ...
- Type 2 diabetes is a disorder characterized by abnormally high levels of blood glucose, also called blood sugar. In this form of diabetes, the body stops ...
- Neurofibromatosis type 2 is a disorder characterized by the growth of noncancerous tumors in the nervous system. The most common tumors associated with neurofibromatosis ...
- 2-hydroxyglutaric aciduria is a condition that causes progressive damage to the brain. The major types of this disorder are called D-2-hydroxyglutaric ...
- Complement component 2 deficiency is a disorder that causes the immune system to malfunction, resulting in a form of immunodeficiency. Immunodeficiencies are conditions ...
- Otopalatodigital syndrome type 2 is a disorder primarily involving abnormalities in skeletal development. It is a member of a group of related conditions called otopalatodigital ...
- 22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by ... of the chromosome at a location designated q11.2.22q11.2 deletion syndrome has many possible signs ...
- Atelosteogenesis type 2 is a severe disorder of cartilage and bone development. Infants born with this condition have very short arms and legs, a narrow chest, and a ...
- Distal myopathy 2 is a condition characterized by weakness of specific muscles that begins in adulthood. It is a form of muscular dystrophy that specifically ...
- Familial cold autoinflammatory syndrome type 2 is a condition that causes episodes of fever, skin rash, and joint pain. These episodes can be triggered by exposure to ...