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Disease Info Card
Classical Phenylketonuria
Information about Classical Phenylketonuria: 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 Classical Phenylketonuria
Most recent studies have shown that Classical Phenylketonuria shares some biological mechanisms with amino-acid-metabolism-inborn-errors, brain-diseases, brain-injuries, cystic-fibrosis, epilepsy, fibrosis, hereditary-diseases, hyperphenylalaninemia, inborn-errors-of-metabolism, malignant-paraganglionic-neoplasm, metabolic-diseases, microcephaly, nervousness, phenylketonuria-ii, phenylketonuria-maternal, phenylketonurias, pregnancy-complications, severe-mental-retardation.
Among the many pathways, these few ones have gauged particular interests from scientists studying Classical Phenylketonuria, and have been seen in publications frequently: Brain Development, Excretion, Gene Conversion, Habituation, Hypersensitivity, Immune Response, Intestinal Absorption, Myelination, Pathogenesis, Phenylalanine Transport, Pigmentation, Regeneration, Regulation Of Gene Expression, Response To Phenylalanine, Reverse Transcription, Secretion, Synaptic Transmission, Translation, Transport, Tryptophan Transport
Quite a number of genes have been found to play important roles in Classical Phenylketonuria, such as ACHE, BLMH, CACNA1A, CSF2, HPSE, IGF1, INS, LAMC2, PAH, PRL, PTS, QDPR, QPCT, SLC25A5, TH, TTR, TYR. 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.