Peripheral axonal atrophy

Symptom Information:

Symptom ID: HPO:0003384
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Peripheral axonal degeneration
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 axonal degeneration(HPO:0000764)
                   Peripheral axonal atrophy(HPO:0003384)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (Orphanet:99946)
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (Orphanet:99947)
Autosomal dominant Charcot-Marie-Tooth disease type 2B (Orphanet:99936)
Autosomal dominant Charcot-Marie-Tooth disease type 2G (Orphanet:99941)
Charcot-Marie-Tooth disease type 2B1 (Orphanet:98856)