Phenotypes for disease #02157 (DDCH (deafness, dystonia, cerebral hypomyelination (DDCH, deletion syndrome, chromosome Xq28)), OMIM:300475)

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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     
0000231725 deafness, dystonia, central hypomyelination, refractory seizure, and fluctuating liver function impairment - - Familial, X-linked - - - - - Ni-Chung Lee 00305878
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