Segmental peripheral demyelination/remyelination
Symptom Information:
Symptom ID: | HPO:0003481 | ||
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) Abnormal peripheral myelination(HPO:0003130) Peripheral demyelination(HPO:0011096) Segmental peripheral demyelination/remyelination(HPO:0003481) MedDRA: |
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Database Frequency: | 12 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A | (Orphanet:100043) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B | (Orphanet:100044) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D | (Orphanet:100046) |
Charcot-Marie-Tooth disease type 1A | (Orphanet:101081) |
Charcot-Marie-Tooth disease type 1C | (Orphanet:101083) |
Charcot-Marie-Tooth disease type 1F | (Orphanet:101085) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Charcot-Marie-Tooth disease type 4D | (Orphanet:99950) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
Hereditary neuropathy with liability to pressure palsies | (Orphanet:640) |
Roussy-Lévy syndrome | (Orphanet:3115) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |