Demyelinating motor neuropathy

Symptom Information:

Symptom ID: HPO:0007220
Synonyms:
Demyelinating motor neuropathy [OMIM:Demyelinating motor neuropathy]
Quality:
Cross references:
OMIM: "Demyelinating motor neuropathy" [OMIM:Demyelinating motor neuropathy]
Is a (Direct Parents):
HPO         Demyelinating peripheral neuropathy
HPO         Motor polyneuropathy
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)
                Peripheral neuropathy(HPO:0009830)
                   Demyelinating peripheral neuropathy(HPO:0007108)
                      Demyelinating motor neuropathy(HPO:0007220)
                   Motor polyneuropathy(HPO:0007178)
                      Demyelinating motor neuropathy(HPO:0007220)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant spastic paraplegia type 36 (Orphanet:320365)
Pelizaeus-Merzbacher-like due to GJC2 mutation (Orphanet:280282)
Spastic paraplegia - neuropathy - poikiloderma (Orphanet:2821)