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Autosomal dominant striatal neurodegeneration
1 OMIM reference -
1 associated gene
1 connected disease
8 signs/symptoms
Disease Type of connection
Primary pigmented nodular adrenocortical disease
Synonym(s):
- ADSD
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: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
PDE8B O95263603390
Very frequent
- Autosomal dominant inheritance
- Elocution disorders / dysarthria / dysphonia
- Execution movement disorder / dysmetria / bradykinesia / akinesia / apraxia
- Movement disorder
- Muscle anomalies

Frequent
- Abnormal gait
- Anomalies of tongue, gingiva and oral mucosa
- Restricted joint mobility / joint stiffness / ankylosis