eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | agenesis of corpus callosum |
| Comorbidity | C0751651|mitochondrial disorder |
| Sentences | 1 |
| PubMedID- 22971091 | We review the axonal charcot-marie-tooth subtypes with onset in infancy, spinal muscular atrophy, and related syndromes of early infancy, giant axonal neuropathy, infantile neuroaxonal dystrophy, hereditary motor and sensory neuropathy with agenesis of the corpus callosum, early-onset neuropathies associated with mitochondrial disorders, and other less well-delineated clinical entities. |
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