Axonal loss

Symptom Information:

Symptom ID: HPO:0003447
Synonyms:
Axonal loss [OMIM:Axonal loss]
Quality:
Cross references:
OMIM: "Axonal loss" [OMIM:Axonal loss]
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 loss(HPO:0003447)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (Orphanet:93114)
CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA (OMIM:212890)
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM (OMIM:118301)
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE (OMIM:118230)
Charcot-Marie-Tooth disease type 4D (Orphanet:99950)
Charcot-Marie-Tooth disease type 4J (Orphanet:139515)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
Muscular dystrophy, Selcen type (Orphanet:199340)
Nasu-Hakola disease (Orphanet:2770)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (Orphanet:308386)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B (Orphanet:308393)