About The Medical Condition Deficiency, Combined Carboxylase
Find the definition of the medical term Deficiency, Combined Carboxylase. Deficiency, Combined Carboxylase defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Deficiency, Combined Carboxylase
| Deficiency, Combined Carboxylase Medical Condition |
|---|
What's The Definition Of The Medical Condition Deficiency, Combined Carboxylase?
A deficiency in the activities of biotin-dependent enzymes (propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to one of two defects in BIOTIN metabolism. The neonatal form is due to HOLOCARBOXYLASE SYNTHETASE DEFICIENCY. The late-onset form is due to BIOTINIDASE DEFICIENCY.
|
More Medical Conditions
A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z
Medical Conditions Definitions Of The Day
- Medigap Policy ‐ A supplemental health insurance policy sold by private insurance…
- Herbal Therapy ‐ Use of plants or herbs to treat diseases or to…
- Test, Lung Function ‐ Measurement of the various processes involved in the act of respiration:…
- Active Biological Transport ‐ The movement of materials across cell membranes and epithelial…
- Mesilate, Deferoxamine ‐ Natural product isolated from Streptomyces pilosus. It forms…
- Collection, Data ‐ Systematic gathering of data for a particular purpose from various…
- Dinitrotoluamide ‐ A coccidiostat…
- Skin Disease, Staphylococcal ‐ Infections to the skin caused by bacteria of the genus…
- Microscopies, SIMS ‐ A mass-spectrometric technique that is used for microscopic chemical…
- Genetic Markers ‐ A phenotypically recognizable genetic trait which can be used…