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Download Data for BH4-deficient hyperphenylalaninemia A
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
This disease has been annotated by GARD as a rare disease.
Description from Mondo Disease Ontology.
Description from UniProt.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0090106
GARD:0005682
MESH:C535325
NCIT:C138171
OMIM:261640
Orphanet:13
SCTID:237914002
UMLS:C0878676
MONDO:0009863
High level summary of knowledge for a disease, including descriptions and datasource references.
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Opens the Target List with this set of targets