eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | rett syndrome |
| Comorbidity | C0003635|apraxia |
| Sentences | 1 |
| PubMedID- 22928142 | A karyotype analysis and molecular testing for angelman syndrome, rett syndrome, and ataxia with oculomotor apraxia type 2 were unrevealing. |
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