hyperammonemia

navigate by keyword : carbamoyl phosphate synthetase deficiency cps1 ammonia anatomy biochemistry biology biotech biotechnology cell diagram disease education enzymatic activity enzyme figure fumarate gene genes genetic disorder genetics genome sciences health human hyperammonemia increased concentrations information inheritable late onset medical medicine metabolic pathway metabolism neonatal screening organ presentation rare science scientific symptoms urea cycle vector

Pink blue ribbon awareness, symbolic bow color for Infant birth defect, Sudden Infant Death Syndrome SIDS Royalty Free Stock Photo

Pink blue ribbon awareness isolated with clipping path bow color for newborn birth defect, Sudden Infant Death Syndrome SIDS, Royalty Free Stock Photo

Pink blue ribbon awareness isolated on white background Clipping path for SID Birth defect illness to end obstetric fistula Royalty Free Stock Photo

Pink blue ribbon awareness isolated clipping path bow for newborn birth defect, Sudden Infant Death Syndrome (SIDS) Royalty Free Stock Photo

Sodium phenylbutyrate urea cycle disorders drug molecule. Also acts as histone acetylase (HDAc) inhibitor and chemical chaperone. Royalty Free Stock Photo

3D image of Carbamoyl phosphate skeletal formula Royalty Free Stock Photo

Carbamoyl Phosphate Synthetase (CPS1) Deficiency vector illustration

Urea Cycle biochemical reaction pathway that produces urea from ammonia Royalty Free Stock Photo

Pink light blue ribbon awareness for Birth defects month, (SIDS) Infertility, Pregnancy Miscarriage, Infant Loss Royalty Free Stock Photo

Argininosuccinic Aciduria ASL Deficiency vector diagram Royalty Free Stock Photo

Arginase ARG1 Deficiency vector diagram illustration Royalty Free Stock Photo

Ornithine Transcarbamylase (OTC) Deficiency diagram vector Royalty Free Stock Photo

Carbamoyl phosphate synthetase I deficiency (CPS1 deficiency) is a genetic disorder that causes episodes of toxic levels of ammonia in the blood (hyperammonemia).