Medicine & Life Sciences
Inborn Urea Cycle Disorder
100%
Neonatal Screening
73%
glycerol phenylbutyrate
59%
Growth Hormone
41%
Inborn Errors Metabolism
34%
Ammonia
27%
Serine Proteinase Inhibitors
24%
Growth Hormone-Releasing Hormone
24%
phenylacetic acid
21%
Mutation
21%
4-phenylbutyric acid
20%
Messenger RNA
20%
Liver
19%
phenylacetylglutamine
18%
Phenotype
17%
Newborn Infant
16%
Genes
15%
Child
14%
Information Systems
13%
Ornithine Carbamoyltransferase Deficiency Disease
13%
Glutamine
12%
Testicular Hormones
12%
Medical Genetics
12%
Homocystinuria
11%
Genetic Counseling
10%
Pediatrics
10%
Phenylketonurias
10%
Pyruvate Dehydrogenase Complex Deficiency Disease
10%
Growth
10%
Insulin-Like Growth Factor I
9%
Medium chain acyl CoA dehydrogenase deficiency
9%
3-methylcrotonyl CoA carboxylase 1 deficiency
9%
Neurofibromatoses
9%
Siblings
9%
Partial deletion Chromosome 11p
9%
Therapeutics
9%
Neurofibromatosis 1
9%
Homocysteine
9%
Argininosuccinate Lyase
8%
Systemic carnitine deficiency
8%
Microcephaly
8%
Hormones
8%
RNA
8%
Biomarkers
7%
Response Elements
7%
Insulin-Like Growth Factor II
7%
Argininosuccinic Aciduria
7%
Databases
7%
Animals
7%
Noonan Syndrome
7%