eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | cogan syndrome |
| Comorbidity | |ataxia |
| Sentences | 52 |
| PubMedID- 22736457 | ataxia with oculomotor apraxia type 1, another recessive ataxia, shares the biochemical features of susceptibility to dna damage with at (for a review, see rass et al., 2007), but also has no clear increased risk of neoplasia (le ber et al., 2003). |
| PubMedID- 19593598 | ataxia with oculomotor apraxia (aoa) type 2 (aoa2 mim 606002) is a recessive subtype of aoa characterized by cerebellar atrophy, oculomotor apraxia, early loss of reflexes, and peripheral neuropathy. |
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