Phenotypes for disease #04503 (DYT2 (dystonia, type 2, torsion, autosomal recessive (DYT-2)), OMIM:224500)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000222494 stiff,Global developmental delay $ limbs spastic cerebral palsy Dystonia Familial, autosomal recessive 03y 05y 01y - - Adel ZEeglam 00288790
0000223293 generalized dystonia spastic cerebral palsy hypermanganesemia Familial, autosomal recessive 05y 03y 03y 03y none Adel ZEeglam 00288790
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