Peripheral hypomyelination
Symptom Information:
Symptom ID: | HPO:0007182 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |