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Infantile dystonia-parkinsonism
1 OMIM reference -
1 associated gene
6 connected diseases
No signs/symptoms info
Disease Type of connection
Young adult-onset Parkinsonism
Parkinsonian-pyramidal syndrome
Cystic fibrosis
Myoclonus-dystonia syndrome
Autosomal dominant macrothrombocytopenia
Romano-Ward syndrome
Synonym(s):
- IPD
- PKDYS
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SLC6A3 Q01959126455
No signs/symptoms info available.