Axonal degeneration/regeneration

Symptom Information:

Symptom ID: HPO:0003378
Synonyms:
Axon degeneration and regeneration [HPO:0003378]
Axonal degeneration/regeneration [OMIM:Axonal degeneration/regeneration]
Quality:
Cross references:
OMIM: "Axonal degeneration/regeneration" [OMIM:Axonal degeneration/regeneration]
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)
                   Axonal degeneration/regeneration(HPO:0003378)
MedDRA:
Database Frequency: 12 / 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)
Autosomal dominant Charcot-Marie-Tooth disease type 2I (Orphanet:99942)
Autosomal dominant Charcot-Marie-Tooth disease type 2J (Orphanet:99943)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A (Orphanet:100043)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D (Orphanet:100046)
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness (Orphanet:101097)
Charcot-Marie-Tooth disease type 2B1 (Orphanet:98856)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
Hereditary motor and sensory neuropathy type 6 (Orphanet:90120)