Segmental peripheral demyelination

Symptom Information:

Symptom ID: HPO:0007107
Synonyms:
Quality:
Cross references:
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(HPO:0007107)
MedDRA:
Database Frequency: 3 / 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)
Charcot-Marie-Tooth disease type 4C (Orphanet:99949)