Demyelinating peripheral neuropathy
Symptom Information:
Symptom ID: | HPO:0007108 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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) MedDRA: |
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Database Frequency: | 8 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Beta-mannosidosis | (Orphanet:118) |
CADASIL | (Orphanet:136) |
Infantile cerebellar-retinal degeneration | (Orphanet:313850) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Spastic paraplegia - neuropathy - poikiloderma | (Orphanet:2821) |