Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
REACTOME PATHWAYThe Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) pathway (Reactome ID: R-HSA-5619081) involves 1 genes and is affected by 70 compounds in the BiohacksAI evidence corpus. Compound-pathway associations are derived from target overlap: a compound is linked to this pathway if it targets ≥2 genes within the pathway.
Genes in this Pathway
Compounds Affecting Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
About the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) Pathway
The Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) pathway is catalogued in Reactome (ID: R-HSA-5619081) and involves 1 genes. In the BiohacksAI corpus, 70 compounds have documented interactions with at least 2 genes in this pathway, establishing mechanistic relevance. Key pathway genes include SLC6A3.