Demyelinating motor neuropathy
Symptom Information:
Symptom ID: | HPO:0007220 | ||||
Synonyms: |
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Is a (Direct Parents): |
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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) Peripheral neuropathy(HPO:0009830) Demyelinating peripheral neuropathy(HPO:0007108) Demyelinating motor neuropathy(HPO:0007220) Motor polyneuropathy(HPO:0007178) Demyelinating motor neuropathy(HPO:0007220) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant spastic paraplegia type 36 | (Orphanet:320365) |
Pelizaeus-Merzbacher-like due to GJC2 mutation | (Orphanet:280282) |
Spastic paraplegia - neuropathy - poikiloderma | (Orphanet:2821) |