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Disease Info Card
Phenylketonuria Ii
Information about Phenylketonuria Ii: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Phenylketonuria Ii
Most recent studies have shown that Phenylketonuria Ii shares some biological mechanisms with basal-ganglia-diseases, brain-diseases, calcinosis, classical-phenylketonuria, dystonia-disorders, epilepsy, folic-acid-deficiency, gtp-cyclohydrolase-i-deficiency, hyperphenylalaninemia, inborn-errors-of-metabolism, malignant-paraganglionic-neoplasm, metabolic-diseases, microcephaly, muscle-hypotonia, nervous-system-disorder, nervousness, phenylketonurias.
Among the many pathways, these few ones have gauged particular interests from scientists studying Phenylketonuria Ii, and have been seen in publications frequently: Aging, Cell Cycle, Demethylation, Endocytosis, Excretion, Hypersensitivity, Intestinal Absorption, Localization, Myelination, Pathogenesis, Pigmentation, Regeneration, Transport, Tryptophan Transport
Quite a number of genes have been found to play important roles in Phenylketonuria Ii, such as CALB2, CD55, CR2, CSF2, CUX1, DHFR, GCH1, HPSE, LAMC2, MECP2, PAH, PRL, PTS, QDPR, SART3, SPR, TH, TPX2. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.
Pathways Related to Phenylketonuria Ii
This information is being compiled and will come in a future update
| Aging | Cell Cycle | Demethylation |
| Endocytosis | Excretion | Hypersensitivity |
| Intestinal Absorption | Localization | Myelination |
| Pathogenesis | Pigmentation | Regeneration |
| Transport | Tryptophan Transport |