Symmetrical progressive peripheral demyelination
Symptom Information:
| Symptom ID: | HPO:0006873 | ||
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Abnormal peripheral nervous system morphology(HPO:0000759) Abnormal peripheral myelination(HPO:0003130) Peripheral demyelination(HPO:0011096) Symmetric peripheral demyelination(HPO:0007262) Symmetrical progressive peripheral demyelination(HPO:0006873) MedDRA: |
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| Database Frequency: | 1 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |