Segmental peripheral demyelination/remyelination

Symptom Information:

Symptom ID: HPO:0003481
Synonyms:
Segmental demyelination/remyelination [HPO:0003481]
Segmental demyelination/remyelination [OMIM:Segmental demyelination/remyelination]
Quality:
Cross references:
OMIM: "Segmental demyelination/remyelination" [OMIM:Segmental demyelination/remyelination]
Is a (Direct Parents):
HPO         Peripheral demyelination
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:
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)