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Disease

Parkinsonism-dystonia, infantile

Also known as IPD, PKDYS, Parkinsonism-dystonia infantile, dopamine transporter deficiency syndrome+1 more

IPD, PKDYS, Parkinsonism-dystonia infantile, dopamine transporter deficiency syndrome, infantile Parkinsonism-dystonia.

2
Associated genes
1
Related proteins

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Associated genes

2 matches

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

SLC6A30.75WARS20.37

Disease biology

1 match

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Sodium-dependent dopamine transportervia SLC6A30.75

Reference

Authoritative identity, definition & identifiers.

Synonyms

IPD, PKDYS, Parkinsonism-dystonia infantile, dopamine transporter deficiency syndrome, infantile Parkinsonism-dystonia

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.