Rare segmental demyelination/remyelination

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Rare segmental demyelination/remyelination" [OMIM:Rare segmental demyelination/remyelination]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2M (Orphanet:228179)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (Orphanet:100044)