3-hydroxy-3-methylglutaric aciduria (3-HMG) is an inherited metabolic disorder caused by a deficiency of the enzyme 3-hydroxy-3-methylglutaryl-CoA lyase (HMGCL). This enzyme is responsible for breaking down certain amino acids and fatty acids in t...

3-hydroxy-3-methylglutaryl-CoA synthase deficiency (HMG-CoA synthase deficiency) is a rare genetic disorder caused by a deficiency of the enzyme 3-hydroxy-3-methylglutaryl-CoA synthase. This enzyme is involved in the production of cholesterol and ...

3-hydroxyisobutyric aciduria is an inherited metabolic disorder caused by a deficiency of the enzyme 3-hydroxyisobutyryl-CoA hydrolase. This enzyme is responsible for breaking down 3-hydroxyisobutyric acid, a byproduct of the metabolism of certain...

3-Methylcrotonyl-CoA carboxylase deficiency is an inherited disorder that affects the body's ability to break down certain proteins. It is caused by a deficiency of the enzyme 3-methylcrotonyl-CoA carboxylase, which is responsible for the breakdow...

3-Methylglutaconic aciduria type 1 (3-MGA type 1) is an inherited metabolic disorder caused by a deficiency of the enzyme 3-methylglutaconyl-CoA hydratase. This enzyme is involved in the breakdown of certain fatty acids and amino acids. People wit...

3-Methylglutaconic aciduria type 3 is a rare inherited metabolic disorder caused by a deficiency of the enzyme 3-methylglutaconyl-CoA hydratase. This enzyme is involved in the breakdown of certain fatty acids and amino acids. People with this diso...

3-Methylglutaconic aciduria type 4 is a rare inherited metabolic disorder caused by a deficiency of the enzyme 3-methylglutaconyl-CoA hydratase. This enzyme is involved in the breakdown of certain fatty acids and amino acids. People with this diso...

3-Methylglutaconic aciduria type 7 (3-MGA type 7) is a rare inherited metabolic disorder caused by a deficiency of the enzyme 3-methylglutaconyl-CoA hydratase (MGCA7). This enzyme is involved in the breakdown of certain fatty acids and amino acids...

3-Methylglutaconic aciduria type 8 (3-MGA type 8) is a rare inherited metabolic disorder caused by a deficiency of the enzyme 3-methylglutaconyl-CoA hydratase (MGCAH). This enzyme is involved in the breakdown of certain fatty acids and amino acids...

3-Methylglutaconic aciduria type 9 (3-MGA type 9) is a rare inherited metabolic disorder caused by a deficiency of the enzyme 3-methylglutaconyl-CoA hydratase (MGCAH). This enzyme is involved in the breakdown of certain fatty acids and amino acids...

3C syndrome is a rare genetic disorder caused by a mutation in the NSD1 gene. It is characterized by craniofacial abnormalities, cardiac defects, and cognitive impairment. Symptoms may include a wide-set eyes, a small jaw, a cleft palate, and hear...

3M syndrome is a rare genetic disorder characterized by short stature, skeletal abnormalities, and facial dysmorphism. It is caused by a mutation in the gene encoding the protein filamin A. Symptoms may include short stature, joint laxity, scolios...

3MC syndrome is a rare genetic disorder that affects the development of multiple body systems. It is characterized by malformations of the head and face, skeletal abnormalities, and intellectual disability. It is caused by a mutation in the gene t...

3p25.3 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the short arm of chromosome 3. It is characterized by intellectual disability, developmental delay, and a variety of physical features. Other feat...

3q13 microdeletion syndrome is a rare genetic disorder caused by a small deletion of genetic material on the long arm of chromosome 3. It is characterized by a variety of physical and developmental abnormalities, including intellectual disability,...

3q26 microduplication syndrome is a rare genetic disorder caused by a small duplication of genetic material on the long arm of chromosome 3. It is characterized by a variety of physical and developmental features, including intellectual disability...

3q26q27 microdeletion syndrome is a rare genetic disorder caused by a deletion of genetic material on the long arm of chromosome 3. It is characterized by intellectual disability, developmental delays, and physical abnormalities. Symptoms can vary...