Peripheral hypomyelination

Symptom Information:

Symptom ID: HPO:0007182
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormal peripheral myelination
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 hypomyelination(HPO:0007182)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Charcot-Marie-Tooth disease type 4A (Orphanet:99948)
Charcot-Marie-Tooth disease type 4E (Orphanet:99951)
Charcot-Marie-Tooth disease type 4G (Orphanet:99953)
Charcot-Marie-Tooth disease type 4J (Orphanet:139515)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
EAST syndrome (Orphanet:199343)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)