Phenotypes for disease #01296 (DYT5 (dystonia, type 5, dopa-responsive type (DYT-5)), OMIM:128230)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Owner     

Individual ID     
0000041541 pure hereditary spastic paraplegia hereditary spastic paraplegia THD Familial, autosomal recessive - - 20y - - Erik-Jan Kamsteeg 00054876
0000242925 HPO´s: (+) Ataxia,(+) Dystonia,(+) Frequent falls,(+) Functional motor deficit,(+) Abnormality of coordination,(+) Abnormality of movement / clinically like segawa dystonia with varying response to L-dopa, predominantly ataxia and falls, clinically significant permanent loss of dopa response and significant ataxia, these and falls are prominent, no PNP, no clear cerebellar signs - - Unknown 56y - - - - Andreas Laner 00324383
0000324433 developmental delay, progressive hypotonia - - Isolated (sporadic) - - - - - Marketa Wayhelova 00434054
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