Childhood-onset benign chorea with striatal involvement




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Total: 0 (papers)
  


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 7

HPO ID Term Frequency
HP:0002072 Chorea Very frequent (99-80%)
HP:0010994 Abnormal corpus striatum morphology Frequent (79-30%)
HP:0031206 Striatal T2 hyperintensity Frequent (79-30%)
HP:0000739 Anxiety Occasional (29-5%)
HP:0002548 Parkinsonism with favorable response to dopaminergic medication Occasional (29-5%)
HP:0000726 Dementia Excluded (0%)
HP:0002194 Delayed gross motor development Excluded (0%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 1

Gene Symbol Gene Name Entrez Gene ID
PDE10A phosphodiesterase 10A 10846